Tag
Inflammation
504 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs1001179 | CAT -262C>T | Catalase promoter variant affecting hydrogen peroxide clearance and antioxida... | Methylation & Detox | Strong | |
| rs10033900 | CFI | Intronic variant in complement factor I associated with age-related macular d... | Longevity & Aging | Strong | |
| rs10045431 | IL12B | Upstream tagging SNP at the IL12B locus that marks the Th1/Th17 risk haplotyp... | Psoriasis & Spondyloarthropathy | Strong | |
| rs1004819 | IL23R | Intronic IL-23 receptor variant that increases susceptibility to ankylosing s... | IBD & Mucosal Immunity | Strong | |
| rs10063949 | SLC23A1 SLC23A1 variant | Intronic variant in the intestinal and renal vitamin C transporter gene (SVCT... | Vitamins & Nutrient Absorption | Moderate | |
| rs10181656 | STAT4 | Intronic STAT4 tagging SNP on the primary SLE risk haplotype; the sentinel va... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs10206753 | IL1RL1 IL1RL1 TIR Domain Risk Haplotype | Missense variant in IL1RL1 encoding the Leu551Ser amino acid change in the in... | Allergy & Atopic Disease | Strong | |
| rs1024611 | CCL2 A-2518G | Promoter variant that increases CCL2 (MCP-1) transcription, amplifying monocy... | Vascular Inflammation & Remodeling | Moderate | |
| rs1036477 | FBN1 | Deep intronic FBN1 variant associated with larger ascending aortic dimensions... | Cardiomyopathy & Structural Heart | Strong | |
| rs1047031 | DEFB1 | 3'UTR variant in the beta-defensin 1 gene that disrupts a microRNA binding si... | Dental & Oral Health | Moderate | |
| rs10499194 | TNFAIP3 | Intergenic regulatory variant at 6q23 near TNFAIP3 whose T allele is protecti... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs10509679 | CYP2C9 | Intronic CYP2C9 haplotype tag associated with increased ischemic stroke risk ... | Coronary Artery Disease & Atherosclerosis | Emerging | |
| rs10050860 | ERAP1 D575N | Missense variant (Asp575Asn) in the ERAP1 catalytic domain that modestly redu... | Psoriasis & Spondyloarthropathy | Strong | |
| rs10167914 | IL1A IL1A Endometriosis Susceptibility Variant | A regulatory tag SNP in the IL1A/IL1B locus on chromosome 2q13; the G allele ... | Endometriosis & Uterine Health | Strong | |
| rs10208293 | IL1RL1 | Intronic IL1RL1 variant tagging an independent regulatory signal at the ST2 l... | Allergy & Atopic Disease | Moderate | |
| rs1041981 | LTA Thr26Asn (TNFB*2) | Missense variant in lymphotoxin-alpha, a TNF superfamily cytokine essential f... | Innate Immunity & Infection Defense | Moderate | |
| rs1049255 | CYBA CYBA 3'UTR A640G | 3'UTR variant in the NADPH oxidase p22-phox subunit affecting superoxide gene... | Vascular Inflammation & Remodeling | Moderate | |
| rs1064793792 | SERPING1 | Frameshift deletion in SERPING1 eliminating C1-inhibitor function — causes he... | B-Cell Immunity & Antibody-Mediated Disease | Established | |
| rs10818488 | TRAF1 TRAF1-C5 rheumatoid arthritis variant | Intergenic regulatory variant between TRAF1 and C5 on chromosome 9; the A all... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs11568821 | LOC105373977 PDCD1/LOC105373977 PD1.3 | Intronic regulatory variant near the PDCD1 (PD-1) immune checkpoint locus tha... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs12640848 | ENAM | Intronic variant in the ENAM enamelin gene associated with altered dental car... | Dental & Oral Health | Moderate | |
| rs10399931 | CHI3L1 CHI3L1 eQTL Partner Variant | Upstream regulatory variant in the CHI3L1 YKL-40 quantitative trait locus; th... | Allergy & Atopic Disease | Moderate | |
| rs104895444 | NOD2 | Rare NOD2 missense variant (Val793Met) identified in IBD deep-resequencing; c... | IBD & Mucosal Immunity | Moderate | |
| rs1048990 | PSMA6 PSMA6 -8C>G | 5'UTR variant that enhances PSMA6 transcription, amplifying proteasome-driven... | Innate Immunity & Infection Defense | Moderate | |
| rs10505806 | MGST1 | Intergenic variant near MGST1 that modifies whether aspirin/NSAIDs reduce col... | Vascular Inflammation & Remodeling | Moderate | |
| rs1054564 | GDF15 GDF15 3'UTR rs1054564 | 3'UTR variant that controls GDF15 expression via microRNA regulation — C alle... | Endometriosis & Uterine Health | Moderate | |
| rs1061170 | CFH Y402H | Strongly increases risk of age-related macular degeneration through impaired ... | Skin & Eyes | Established | |
| rs1064793917 | SERPING1 | Frameshift deletion in SERPING1 (p.Lys390fs) abolishing C1-inhibitor producti... | B-Cell Immunity & Antibody-Mediated Disease | Established | |
| rs10984447 | DBC1 DBC1 multiple sclerosis susceptibility variant | Intronic variant in DBC1 (DBCCR1/BRINP1) at 9q33.1 associated with multiple s... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs11265611 | IL6R | Intronic IL6R variant in LD with the IL-6 receptor signaling locus; G allele ... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs11652075 | CARD14 CARD14 Arg820Trp (R820W) | Missense variant in the keratinocyte NF-κB scaffold protein CARD14 that modes... | Psoriasis & Spondyloarthropathy | Strong | |
| rs12101255 | TSHR | Intronic regulatory variant in TSHR intron 1; the T allele disrupts thymic ex... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs12232375 | ZFPM1 ZFPM1 Hematology/Cardiac Locus Variant | Intronic ZFPM1 variant tagging reduced GATA cofactor regulatory activity; the... | Arrhythmia & Heart Rhythm | Strong | |
| rs1537415 | GLT6D1 | Intronic variant in GLT6D1 reducing GATA-3 transcription factor binding in T ... | Dental & Oral Health | Strong | |
| rs1050152 | SLC22A4 OCTN1 L503F | Missense variant in SLC22A4 encoding the organic cation/ergothioneine transpo... | Allergy & Atopic Disease | Strong | |
| rs10507391 | ALOX5AP SG13S114 intron variant | Intronic ALOX5AP variant in the HapA haplotype; the A allele is associated wi... | Vascular Inflammation & Remodeling | Moderate | |
| rs10738445 | BNC2 BNC2 AIS susceptibility variant | Intronic enhancer variant in basonuclin-2 that increases YY1 binding and BNC2... | Innate Immunity & Infection Defense | Strong | |
| rs10800309 | FCGR2A FCGR2A intronic variant | Intronic upstream variant in FCGR2A that modulates surface expression of the ... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs10859871 | VEZT | Intronic variant near the VEZT (vezatin) gene at 12q22 associated with increa... | Endometriosis & Uterine Health | Strong | |
| rs10954213 | IRF5 3'UTR polyadenylation | 3'UTR variant creating a functional polyadenylation site; A allele produces a... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs1143627 | IL1B -31T>C | Promoter variant that elevates IL-1β transcription, increasing risk of H. pyl... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs11556924 | ZC3HC1 R363H | Missense variant in ZC3HC1/NIPA altering cell cycle regulation; the T (His363... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs11726117 | ALPK1 ALPK1 variant | Missense variant in the innate immune kinase ALPK1 (Met861Thr); the C allele ... | Uric Acid & Kidney Function | Moderate | |
| rs12188300 | IL12B | Near-gene variant at the IL12B locus associated with psoriasis risk through a... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs17175830 | ZFPM1 ZFPM1 intronic variant | Intronic variant in ZFPM1 (FOG1), the master transcriptional co-regulator of ... | Arrhythmia & Heart Rhythm | Strong | |
| rs10489629 | IL23R | Intronic IL23R variant in LD block 2 where the T allele is associated with in... | IBD & Mucosal Immunity | Strong | |
| rs10751659 | PRG3 PRG3 Eosinophil Major Basic Protein Homologue Variant | Intronic variant in the PRG3 gene encoding eosinophil major basic protein hom... | Allergy & Atopic Disease | Emerging | |
| rs10759931 | TLR4 -2604G>A | Promoter variant in Toll-like receptor 4 that drives higher TLR4 expression a... | Innate Immunity & Infection Defense | Moderate | |
| rs10882398 | PLCE1 | Intronic PLCE1 variant where the A allele raises systolic blood pressure and ... | Blood Pressure & Hypertension | Strong | |
| rs11264799 | FCRL3 | Upstream regulatory variant in FCRL3 with a strong eQTL effect on FCRL3 expre... | B-Cell Immunity & Antibody-Mediated Disease | Emerging | |
| rs11269962 | IRF5 Regulatory | A 14-bp indel 2.2 kb upstream of IRF5 that is the most strongly associated ci... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs1143634 | IL1B +3954C>T | Synonymous exon 5 variant in IL-1β that increases IL-1β protein secretion des... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs11881940 | HNRNPUL1 | Intronic variant in HNRNPUL1, an RNA-processing gene highly expressed in macr... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs198968 | KLK4 | Intronic variant in kallikrein-related peptidase 4 gene affecting KLK4 expres... | Dental & Oral Health | Moderate | |
| rs104894664 | TTR Ala45Thr (A25T) | Rare pathogenic TTR missense variant causing hereditary transthyretin amyloid... | Cardiomyopathy & Structural Heart | Strong | |
| rs10980705 | LPAR1 | Upstream regulatory variant that increases LPAR1 transcriptional activity in ... | Fitness & Body | Emerging | |
| rs11071559 | RORA | Intronic variant in the circadian clock regulator RORA; the T allele is prote... | Allergy & Atopic Disease | Moderate | |
| rs12095080 | DIO1 DIO1 cardiac mortality variant | 3' UTR variant in the type 1 deiodinase gene associated with markedly increas... | Coronary Artery Disease & Atherosclerosis | Emerging | |
| rs1234314 | TNFSF4 | Intronic variant in TNFSF4 that reduces OX40 ligand promoter activity and is ... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs1250248 | FN1 | Intronic variant in the fibronectin 1 gene associated with increased suscepti... | Endometriosis & Uterine Health | Strong | |
| rs1270942 | CFB | Intronic variant in Complement Factor B associated with strongly elevated sys... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs12720270 | TYK2 TYK2 Intron 7 Splicing Variant | An intronic variant in TYK2 intron 7 that promotes exon 8 inclusion in the ma... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs12883343 | NFKBIA NFKBIA/IkB-alpha variant | Regulatory variant near NFKBIA that specifically elevates risk for psoriatic ... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs13207033 | TNFAIP3 | Intergenic protective variant near TNFAIP3 that tags a haplotype associated w... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs1378577 | ABCG1 ABCG1 ischemic stroke variant | Regulatory variant ~2kb upstream of ABCG1 that modulates transporter expressi... | Atherogenic Lipoproteins | Moderate | |
| rs10889160 | CYP2J2 | Intronic CYP2J2 tag SNP; the C allele marks a haplotype associated with reduc... | Vascular Inflammation & Remodeling | Moderate | |
| rs10889677 | IL23R | 3' UTR and intronic IL23R variant disrupting Let-7e/Let-7f miRNA binding — th... | IBD & Mucosal Immunity | Strong | |
| rs11079788 | TBX21 TBX21 Regulatory Variant | Intronic regulatory variant in TBX21 that influences T-bet expression and Th1... | Allergy & Atopic Disease | Emerging | |
| rs11959928 | DAB2 | Intronic regulatory variant that increases DAB2 expression in kidney tubules,... | Cholesterol & Lipoproteins | Strong | |
| rs1256335 | ALPL | Intronic variant near ALPL associated with increased alkaline phosphatase act... | Vitamins & Nutrient Absorption | Strong | |
| rs12720356 | TYK2 Ile684Ser | A missense variant in the TYK2 pseudokinase (JH2) domain that partially impai... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs13190932 | TRAF3IP2 R74W | Missense variant in the IL-17 adaptor Act1 (Arg74Trp) that is the primary GWA... | Psoriasis & Spondyloarthropathy | Strong | |
| rs13245639 | IRF5 Regulatory | Cis-regulatory IRF5 variant in near-perfect LD (r²=0.97) with the rs729302 pr... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs17561 | IL1A Ala114Ser | Missense variant in IL-1α (Ala114Ser) that acts as a common hypomorphic mutat... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs2235373 | IRF6 | Intronic IRF6 variant associated with non-syndromic cleft lip with or without... | Dental & Oral Health | Moderate | |
| rs1058932 | CYP2C8 | CYP2C8 3-prime UTR variant associated with cardiovascular risk via altered ep... | Pharmacogenomics | Moderate | |
| rs10958409 | SOX17 | Intergenic variant near SOX17 at 8q11 that reduces expression of this endothe... | Vascular Inflammation & Remodeling | Strong | |
| rs11052552 | CLECL1 | Intronic variant in CLECL1, a dendritic-cell costimulatory C-type lectin, ass... | Appetite & Obesity | Moderate | |
| rs11204971 | FLG FLG locus regulatory variant | Regulatory tag SNP in the filaggrin (FLG) locus associated with reduced FLG e... | Allergy & Atopic Disease | Moderate | |
| rs11209026 | IL23R R381Q | Strongly protective variant against inflammatory bowel disease and other auto... | IBD & Mucosal Immunity | Established | |
| rs12700667 | 7p15.2 (near HOXA10/HOXA11) | Intergenic GWAS locus upstream of homeobox genes HOXA10 and HOXA11 that may i... | Endometriosis & Uterine Health | Established | |
| rs12722489 | IL2RA | Intronic variant in IL2RA intron 1 that creates an estrogen-responsive enhanc... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs13193677 | TRAF3IP2 | Intronic variant near the TRAF3IP2 locus (annotated in IPCEF1 at chr6q25.2 by... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs17881320 | STAT3 JAK-STAT3 Signaling Variant | Intronic STAT3 variant associated with increased atopic dermatitis risk (OR=1... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs1800871 | IL10 -819 C>T | Promoter variant in the IL-10 haplotype system — regulates IL-10 anti-inflamm... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs10519177 | FBN1 | Intronic FBN1 variant that requires two copies of the G allele to impair fibr... | Cardiomyopathy & Structural Heart | Emerging | |
| rs11229030 | PRG2 | Intergenic tag SNP in the PRG2/PRG3 eosinophil major basic protein gene clust... | Allergy & Atopic Disease | Moderate | |
| rs11572325 | CYP2J2 | Intronic CYP2J2 variant associated with increased myocardial infarction risk ... | Vascular Inflammation & Remodeling | Moderate | |
| rs11842874 | MCF2L | Intronic variant in MCF2L that acts as a synovial eQTL — A allele carriers ha... | Fitness & Body | Strong | |
| rs121918393 | APOE Christchurch (R136S) | Ultra-rare APOE3 missense variant that dramatically reduces HSPG binding and ... | Longevity & Aging | Strong | |
| rs13196377 | TRAF3IP2 Intronic haplotype member | Intronic tagging variant in the TRAF3IP2/TRAF3IP2-AS1 locus that distinguishe... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs13324341 | MRAS | Intronic MRAS variant that creates a MEF2 transcription factor binding site i... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs150597413 | FLG S3247X | Nonsense variant eliminating filaggrin protein — a minor European FLG null al... | Skin & Eyes | Strong | |
| rs1799724 | TNF -857C>T | TNF promoter variant that disrupts an OCT-1 binding site, altering TNF-alpha ... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs1800787 | FGB -148C>T | Upstream promoter variant in fibrinogen beta chain that elevates circulating ... | Coagulation & Clotting Factors | Strong | |
| rs1800896 | IL10 -1082 A>G | Promoter variant affecting IL-10 production — the master anti-inflammatory cy... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs1801274 | FCGR2A H131R | Missense variant in Fc gamma receptor IIa that substitutes histidine (H131, h... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs2274327 | CA6 Thr55Met | Reduces salivary carbonic anhydrase VI (gustin) secretion, impairing oral aci... | Dental & Oral Health | Moderate | |
| rs11236797 | LRRC32 | Regulatory variant in a distal enhancer at 11q13.5 that controls GARP express... | Allergy & Atopic Disease | Strong | |
| rs11465770 | IL23R | Intronic IL23R variant whose minor T allele tags a protective haplotype that ... | IBD & Mucosal Immunity | Moderate | |
| rs1154155 | TRA | T-cell receptor alpha locus variant associated with narcolepsy susceptibility... | Hormones & Sleep | Strong | |
| rs11967262 | VEGFA | Regulatory variant ~7 kb upstream of VEGFA linked to elevated varicose vein r... | Vascular Inflammation & Remodeling | Moderate | |
| rs12206094 | FOXO3 | Functional FOXO3 intronic variant with allele-specific CTCF binding and IGF-1... | Longevity & Aging | Strong | |
| rs13210247 | TRAF3IP2 | Intronic variant in the TRAF3IP2 locus that lies within the antisense lncRNA ... | Psoriasis & Spondyloarthropathy | Strong | |
| rs1535 | FADS2 | Intronic FADS2 variant with stronger independent associations than rs174575 f... | Triglycerides & Fatty Acids | Strong | |
| rs1800629 | TNF -308 G>A | Promoter variant increasing TNF-alpha production approximately 2-fold, associ... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs1800788 | FGB -854G>A | Upstream promoter variant in fibrinogen beta chain that increases IL-6-driven... | Coagulation & Clotting Factors | Moderate | |
| rs1861494 | IFNG IFNG Interferon Gamma | Intronic IFNG variant that modulates interferon-gamma expression, with the T ... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs1883832 | CD40 Kozak -1C>T | Kozak sequence variant at position −1 of the CD40 start codon — the C allele ... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs2738058 | DEFA1A3 | Intergenic variant downstream of the DEFA1A3 alpha-defensin locus; T risk all... | Dental & Oral Health | Strong | |
| rs11465804 | IL23R | Intronic IL23R variant in strong linkage disequilibrium with the functional R... | IBD & Mucosal Immunity | Strong | |
| rs11466750 | TSLP 3'UTR Splice Variant | 3'UTR variant in TSLP that acts as an eQTL driving higher TSLP mRNA expressio... | Allergy & Atopic Disease | Moderate | |
| rs1205 | CRP +1846C>T | 3' UTR variant that modulates baseline C-reactive protein levels and inflamma... | Vascular Inflammation & Remodeling | Strong | |
| rs12212067 | FOXO3 | Intronic FOXO3 variant whose minor G allele creates an MZF1 transcription fac... | Longevity & Aging | Strong | |
| rs1539243 | IKBKE IKBKE Ile67 synonymous variant | Synonymous coding variant in exon 4 of IKBKE (IKK-epsilon); the C allele tags... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs16840252 | CTLA4 | Upstream promoter variant (~1147 bp 5' of CTLA4) tagging an autoimmune-associ... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs1800630 | TNF -863C>A | TNF promoter variant that disrupts NF-κB p50-p50 binding, reducing TNF-alpha ... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs1800789 | FGB -249G>A | Upstream promoter variant in fibrinogen beta chain that is associated with lo... | Coagulation & Clotting Factors | Moderate | |
| rs1990760 | IFIH1 Ala946Thr | Gain-of-function missense variant in the MDA5 viral RNA sensor, enhancing typ... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs201363394 | SERPING1 Arg400Cys | Pathogenic missense variant in SERPING1 encoding C1-inhibitor; the Arg400Cys ... | B-Cell Immunity & Antibody-Mediated Disease | Established | |
| rs2911463 | PIEZO1 | Intronic variant in PIEZO1, the endothelial mechanosensory ion channel that s... | Arrhythmia & Heart Rhythm | Strong | |
| rs115161931 | CTSS | Independent CTSS-locus GWAS signal for atopic dermatitis on chromosome 1q21.3... | Allergy & Atopic Disease | Moderate | |
| rs12044149 | IL23R | Regulatory variant upstream of the IL-23 receptor gene more strongly associat... | IBD & Mucosal Immunity | Strong | |
| rs1360590 | CDKN2BAS | Intronic variant in ANRIL at the 9p21.3 locus — the shared susceptibility reg... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs17085007 | USP12 | Regulatory variant at the chromosome 13q12 locus that tags a region upstream ... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs17482078 | ERAP1 R725Q | Missense variant (Arg725Gln) in the ERAP1 peptide-binding domain that reduces... | Psoriasis & Spondyloarthropathy | Strong | |
| rs1800790 | FGB -455G>A | Promoter variant in the fibrinogen beta-chain gene that upregulates FGB trans... | Coagulation & Clotting Factors | Strong | |
| rs187084 | TLR9 Promoter -1486T/C | Promoter variant that alters transcription factor binding and TLR9 expression... | Innate Immunity & Infection Defense | Moderate | |
| rs2004640 | IRF5 G198T | Intronic variant creating alternative splice site that increases type I inter... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs201408742 | GPR174 | X-linked intergenic variant near GPR174 (G protein-coupled receptor 174), a l... | TNF, NF-kB & Inflammatory Cytokines | Emerging | |
| rs11136000 | CLU | Intronic variant in clusterin gene affecting Alzheimer's disease risk through... | Neurology & Cognition | Established | |
| rs1154404 | ADH5 ADH5 Asthma Risk Haplotype Variant | Intronic variant in ADH5 (GSNOR) in near-complete LD (r²=0.99) with adjacent ... | Allergy & Atopic Disease | Moderate | |
| rs11590235 | SKI | TGF-beta signaling regulator variant identified as the top shared locus betwe... | Cardiomyopathy & Structural Heart | Moderate | |
| rs13107325 | SLC39A8 A391T | Zinc and manganese transporter variant that reduces metal ion absorption, aff... | IBD & Mucosal Immunity | Strong | |
| rs142885915 | NPSR1 NPSR1 Endometriosis Risk Variant | An intronic insertion/deletion variant in the neuropeptide S receptor 1 gene ... | Endometriosis & Uterine Health | Moderate | |
| rs1501299 | ADIPOQ +276G>T | Intronic variant in the adiponectin gene that influences circulating adiponec... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs17166496 | FSTL4 FSTL4 rs17166496 | Intronic variant in FSTL4 (Follistatin-Like 4) on chromosome 5q31; heterozygo... | Appetite & Obesity | Emerging | |
| rs17728338 | TNIP1 TNIP1/ABIN1 variant | Intergenic regulatory variant near TNIP1 whose A allele reduces ABIN1-mediate... | Psoriasis & Spondyloarthropathy | Strong | |
| rs179247 | TSHR TSHR Intron 1 Graves' Disease Risk Variant | Intronic regulatory variant in TSHR intron 1; the A allele reduces thymic exp... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs1801020 | F12 46C>T | 5' UTR variant that reduces Factor XII translation efficiency, lowering plasm... | Coagulation & Clotting Factors | Moderate | |
| rs1898830 | TLR2 | Intronic TLR2 variant that modulates innate immune signaling intensity; G all... | Innate Immunity & Infection Defense | Moderate | |
| rs2043211 | CARD8 C10X | Truncating variant in the NLRP3 inflammasome brake that abolishes CARD8's cas... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs2269475 | AIF1 AIF1 Arg69Trp | Missense variant in allograft inflammatory factor 1 (Iba1), a macrophage-expr... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs2288904 | SLC44A2 R154Q | Missense variant that impairs platelet-neutrophil binding and blocks flow-dep... | Von Willebrand & Anticoagulant Proteins | Strong | |
| rs11650354 | TBX21 TBX21 Region Variant | Intronic variant in TBX21 that forms a risk haplotype with rs16947078; the T ... | Allergy & Atopic Disease | Strong | |
| rs128627256 | DMD Arg2905Ter (R2905X) | Nonsense variant in dystrophin that eliminates full-length protein, causing X... | Cardiomyopathy & Structural Heart | Established | |
| rs13217795 | FOXO3 | Original 2008 Willcox longevity discovery variant; C allele tags the protecti... | Longevity & Aging | Strong | |
| rs13900 | CCL2 CCL2 3'UTR variant | 3'UTR variant that increases CCL2 mRNA stability via enhanced HuR binding, el... | Vascular Inflammation & Remodeling | Moderate | |
| rs17228212 | SMAD3 | Intronic variant in the TGF-beta signaling gene SMAD3 associated with vascula... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs2066808 | IL23A | Intronic variant near IL23A encoding the IL-23 p19 subunit; G allele increase... | Psoriasis & Spondyloarthropathy | Strong | |
| rs2104286 | IL2RA | Intronic variant affecting IL-2 receptor alpha chain expression and soluble I... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs2105325 | LOC100506023 LOC100506023 rs2105325 | Intronic variant in LOC100506023 (PRDX6-AS1) and TNFSF4 at the 1q25.1 locus, ... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs2234067 | ETV7 ETV7 rs2234067 | Upstream regulatory variant near ETV7, an interferon-inducible transcriptiona... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs4225 | APOC3 APOC3 3'UTR c.*71G>T | 3'UTR variant that creates a microRNA-4271 binding site; the T allele suppres... | Atherogenic Lipoproteins | Moderate | |
| rs11650680 | ORMDL3 ORMDL3 17q21 asthma susceptibility | Intronic regulatory variant in the ORMDL3 17q21 haploblock; the C allele driv... | Allergy & Atopic Disease | Strong | |
| rs1343151 | IL23R | Intronic IL23R variant whose minor A allele tags the protective haplotype for... | IBD & Mucosal Immunity | Moderate | |
| rs143383 | GDF5 C/T | Regulatory variant in GDF5 affecting cartilage development and osteoarthritis... | Fitness & Body | Established | |
| rs1537377 | CDKN2BAS CDKN2B-AS1 rs1537377 | Regulatory variant in the ANRIL long non-coding RNA at the 9p21.3 locus; the ... | Endometriosis & Uterine Health | Strong | |
| rs16944 | IL1B -511C>T | Promoter variant affecting IL-1 beta production, influencing inflammatory res... | Vascular Inflammation & Remodeling | Strong | |
| rs1746048 | CXCL12 | Regulatory variant 80 kb downstream of CXCL12 on chromosome 10q11; the T alle... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs2066865 | FGG 10034C>T | 3' region variant in the fibrinogen gamma chain gene that shifts the gamma/ga... | Coagulation & Clotting Factors | Strong | |
| rs2108225 | SLC26A3 SLC26A3 Ulcerative Colitis Susceptibility Variant | Regulatory variant at the SLC26A3 locus associated with ulcerative colitis su... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs2201841 | IL23R | Intronic variant in the IL-23 receptor gene associated with increased risk of... | Psoriasis & Spondyloarthropathy | Strong | |
| rs2230199 | C3 R102G | Missense variant in complement C3 increasing risk of age-related macular dege... | Skin & Eyes | Established | |
| rs2230600 | PTPN13 I1522M | Missense variant in PTPN13 (FAP-1) converting Ile to Met at position 1522; th... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs2280714 | IRF5 3'UTR | Downstream regulatory variant in the IRF5 3' region that elevates IRF5 mRNA e... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs28929454 | SERPINA1 | SERPINA1 intronic variant strongly associated with elevated mortality in ANCA... | B-Cell Immunity & Antibody-Mediated Disease | Emerging | |
| rs4253623 | PPARA | Intronic PPARA variant whose minor G allele has been associated with modest m... | Atherogenic Lipoproteins | Emerging | |
| rs11657479 | TBX21 TBX21 3' UTR Variant | A 3' UTR variant in TBX21 (c.*169T>C) that modulates T-bet expression; the C ... | Allergy & Atopic Disease | Moderate | |
| rs1495965 | IL23R | Intergenic variant between IL23R and IL12RB2 on chromosome 1p31.3 associated ... | IBD & Mucosal Immunity | Strong | |
| rs1524107 | IL6 | Intronic IL6 variant tagging a low-producing haplotype — the T allele is prot... | Longevity & Aging | Moderate | |
| rs17222814 | ALOX5AP SG13S114 (HapB tag) | Intronic ALOX5AP variant tagging the HapB risk haplotype; the A allele marks ... | Vascular Inflammation & Remodeling | Moderate | |
| rs17465637 | MIA3 | Intronic variant in MIA3/TANGO1 affecting collagen secretion and vascular smo... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs1903068 | KDR KDR/VEGFR2 Endometriosis Angiogenesis Variant | Intergenic variant ~17 kb upstream of KDR (encoding VEGFR2, the primary VEGF ... | Endometriosis & Uterine Health | Strong | |
| rs2230926 | TNFAIP3 F127C | Missense variant in the A20 ubiquitin-editing enzyme that weakens NF-kB negat... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs2256774 | IL2RA | Intronic IL2RA variant that modulates soluble IL-2RA shedding and Treg signal... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs230523 | NFKB1 | Intronic variant in the master immune transcription factor NF-κB1, associated... | Innate Immunity & Infection Defense | Strong | |
| rs2364480 | LTBR | Synonymous coding variant in the lymphotoxin-beta receptor gene associated wi... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs2731672 | F12 | Regulatory tag variant in the Factor XII locus associated with plasma FXII ac... | Coagulation & Clotting Factors | Strong | |
| rs3024491 | IL10 Intronic variant | Intronic IL10 variant that reduces anti-inflammatory cytokine production, ind... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs11808092 | EVI5 | Missense variant in EVI5's coiled-coil domain altering immune cell traffickin... | Neurology & Cognition | Strong | |
| rs12123821 | FLG Filaggrin skin barrier variant | Common regulatory variant in the FLG locus associated with impaired skin barr... | Allergy & Atopic Disease | Strong | |
| rs17222842 | ALOX5AP ALOX5AP variant (SG13S32) | Intronic ALOX5AP haplotype tag; the common G allele marks the HapB cardiovasc... | Vascular Inflammation & Remodeling | Moderate | |
| rs17514846 | FURIN | Intronic regulatory variant modulating FURIN expression via allele-specific D... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs1800972 | DEFB1 DEFB1 -44C>G | Promoter variant in the beta-defensin 1 gene that reduces constitutive hBD-1 ... | IBD & Mucosal Immunity | Moderate | |
| rs2233434 | NFKBIE | Missense variant in NFKBIE (IκBε) reducing the inhibitory capacity of the IκB... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs2268458 | TSHR TSHR Intron 1 Meta-Analysis Variant | Intronic variant in TSHR intron 1; the C allele increases susceptibility to G... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs2546890 | LOC285626 LOC285626 rs2546890 | Regulatory variant upstream of IL12B associated with increased risk of multip... | Psoriasis & Spondyloarthropathy | Strong | |
| rs2569190 | CD14 -159C>T | Promoter variant affecting CD14 expression and LPS receptor signaling — deter... | Innate Immunity & Infection Defense | Strong | |
| rs3024505 | IL10 3' downstream variant | Downstream IL10 enhancer variant that disrupts a STAT3 binding site, reducing... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs3126085 | FLG | Intronic regulatory variant in the filaggrin gene locus that reduces FLG expr... | Skin & Eyes | Strong | |
| rs4220 | FGB Arg448Lys (R448K) | Missense variant in the fibrinogen beta chain that elevates circulating fibri... | Coagulation & Clotting Factors | Moderate | |
| rs5128 | APOC3 3238C>G (SstI) | Regulates triglyceride metabolism through effects on APOC3 expression in the ... | Atherogenic Lipoproteins | Strong | |
| rs12133641 | IL6R IL-6 receptor intronic variant | Deep intronic IL6R variant associated with atopic dermatitis risk and systemi... | Allergy & Atopic Disease | Strong | |
| rs12979860 | IFNL4 | Intronic variant in IFNL4 — the strongest host genetic predictor of hepatitis... | Pharmacogenomics | Established | |
| rs149007883 | NFKBIZ NFKBIZ p.Gly102Ala | Rare protective missense variant in the NF-kB inhibitor zeta gene that reduce... | Hormones & Sleep | Moderate | |
| rs17147230 | IL6 | Near-gene upstream variant in IL6 associated with hepatocellular carcinoma ri... | Longevity & Aging | Moderate | |
| rs17576 | MMP9 MMP9 Q279R | Missense variant in the MMP9 fibronectin type II domain affecting matrix meta... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs17697419 | VEGFC | Intronic variant in the primary lymphangiogenesis growth factor gene; the min... | Vascular Inflammation & Remodeling | Moderate | |
| rs2234663 | IL1RN | Intron 2 VNTR polymorphism in IL1RN that alters IL-1Ra isoform balance and is... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs2304256 | TYK2 TYK2 V362F | A common missense and splicing variant in TYK2 that promotes exon 8 inclusion... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs26653 | ERAP1 | Missense variant (Arg127Pro) in ERAP1 that subtly alters ER peptide trimming ... | Psoriasis & Spondyloarthropathy | Strong | |
| rs28362491 | NFKB1 -94ins/delATTG | Promoter insertion/deletion polymorphism reducing NF-κB p50 transcription and... | Innate Immunity & Infection Defense | Strong | |
| rs3738919 | ITGAV ITGAV integrin alpha-V variant | Intronic ITGAV variant associated with rheumatoid arthritis susceptibility in... | B-Cell Immunity & Antibody-Mediated Disease | Emerging | |
| rs12141494 | CHI3L1 CHI3L1 Intron 6 Variant | Intronic variant in CHI3L1 (intron 6) independently associated with asthma se... | Allergy & Atopic Disease | Moderate | |
| rs12980275 | IFNL3 | Downstream variant near IFNL3 — third IL28B locus predictor of hepatitis C sp... | Pharmacogenomics | Established | |
| rs174553 | FADS1 | Intronic variant in the FADS1 gene cluster that reduces delta-5 desaturase ac... | Triglycerides & Fatty Acids | Strong | |
| rs17697515 | VEGFC | Intronic VEGFC variant independently associated with reduced diabetic retinop... | Vascular Inflammation & Remodeling | Moderate | |
| rs1805762 | M6PR | Intronic M6PR variant associated with modest hypertension risk in East Asian ... | Coronary Artery Disease & Atherosclerosis | Emerging | |
| rs2275913 | IL17A -197G>A | Promoter variant in the NFAT binding site that increases IL-17A transcription... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs231775 | CTLA4 Thr17Ala | Missense variant in the CTLA-4 leader peptide that reduces surface expression... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs27044 | ERAP1 Gln730Glu | Missense variant in the ERAP1 C-terminal regulatory domain modulating peptide... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs3131379 | MSH5 | Intronic variant in the HLA class III region near MSH5 associated with lupus ... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs4253238 | KLKB1 KLKB1 intronic variant | Intronic KLKB1 variant whose T allele elevates plasma kallikrein enzymatic ac... | Coagulation & Clotting Factors | Moderate | |
| rs5177 | LRP8 LRP8 3'UTR variant | 3'UTR variant in LRP8 (ApoER2) that affects mRNA stability and forms part of ... | Atherogenic Lipoproteins | Moderate | |
| rs641738 | MBOAT7 | Regulatory variant that reduces MBOAT7 expression in the liver, impairing pho... | Liver Fat | Strong | |
| rs12053868 | IL1RAP IL1RAP amyloid risk variant | Intronic variant in IL1RAP that impairs microglial activation, accelerating b... | Neurology & Cognition | Moderate | |
| rs12251307 | IL2RA IL-2 receptor alpha chain variant | Intergenic variant 19 kb downstream of IL2RA associated with atopic dermatiti... | Allergy & Atopic Disease | Strong | |
| rs1799987 | CCR5 CCR5 Promoter -2459A>G | Regulatory variant in the CCR5 promoter that reduces CCR5 expression by ~45%;... | Vascular Inflammation & Remodeling | Moderate | |
| rs231806 | CTLA4 | Upstream regulatory variant in the CTLA4 MH30 region associated with latent a... | Autoimmune Tolerance & T-Cell Regulation | Emerging | |
| rs27524 | ERAP1 | Intronic ERAP1 variant that increases expression, raising psoriasis risk spec... | Psoriasis & Spondyloarthropathy | Strong | |
| rs352140 | TLR9 | Synonymous variant in TLR9 that increases receptor expression, amplifying inn... | Innate Immunity & Infection Defense | Moderate | |
| rs397507563 | FLG 3702delG | Frameshift deletion in the third filaggrin repeat domain — the third most com... | Skin & Eyes | Established | |
| rs419788 | SKIV2L | Intronic SKIV2L variant in the MHC class III region; the T allele tags an ind... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs12368672 | STAT6 STAT6 intronic variant | Deep intronic variant in STAT6 that modulates IL-4/IL-13 signal transduction;... | Allergy & Atopic Disease | Moderate | |
| rs174568 | FADS2 FADS2 C>T (delta-6 desaturase) | Intronic regulatory variant in FADS2 encoding delta-6 desaturase, the rate-li... | Triglycerides & Fatty Acids | Moderate | |
| rs17493811 | AGER | Tag SNP in the AGER 3′ downstream region associated with increased type 1 dia... | Hormones & Sleep | Moderate | |
| rs1800471 | TGFB1 R25P (Arg25Pro) | Signal-peptide missense variant altering TGF-β1 secretion levels, associated ... | Vascular Inflammation & Remodeling | Moderate | |
| rs1935949 | FOXO3 | Second independent FOXO3 longevity signal tagging a distinct intronic haploty... | Longevity & Aging | Moderate | |
| rs2231137 | ABCG2 ABCG2 V12M (Val12Met) | Missense variant in the ABCG2 transporter that impairs membrane localization ... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs2469434 | CD226 | Deep-intronic variant in the CD226 (DNAM-1) co-stimulatory receptor gene asso... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs2501401 | CNR2 | Intronic eQTL in CNR2 (cannabinoid receptor 2) that modulates receptor expres... | TNF, NF-kB & Inflammatory Cytokines | Emerging | |
| rs2856836 | IL1A | 3' UTR variant in IL1A (interleukin-1 alpha) associated with endometriosis su... | Endometriosis & Uterine Health | Moderate | |
| rs30187 | ERAP1 K528R | Missense variant reducing ERAP1 aminopeptidase activity, increasing ankylosin... | Psoriasis & Spondyloarthropathy | Strong | |
| rs4151667 | CFB L9H | Missense variant in the signal peptide of complement factor B forming the H10... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs4728142 | IRF5 Promoter Indel Tag (CGGGG insertion) | Enhancer variant ~5 kb upstream of IRF5 that promotes ZBTB3-mediated chromati... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs6834314 | HSD17B13 | Intergenic tag SNP in near-perfect linkage disequilibrium with the HSD17B13 s... | Liver Fat | Moderate | |
| rs11683424 | DNMT3A | Intronic variant in the de novo DNA methyltransferase DNMT3A, associated with... | Methylation & Detox | Emerging | |
| rs12551256 | IL33 IL33 protective asthma variant | Intronic IL33 variant where the G allele is negatively associated with asthma... | Allergy & Atopic Disease | Emerging | |
| rs13412852 | LPIN1 | Intronic variant in LPIN1 (lipin-1) associated with liver fat accumulation an... | Fat Storage & Energy | Emerging | |
| rs1800872 | IL10 -592 C>A | Promoter variant affecting IL-10 production — a key anti-inflammatory cytokin... | Vascular Inflammation & Remodeling | Strong | |
| rs2241766 | ADIPOQ T45G | Synonymous exon 2 variant in the adiponectin gene that affects mRNA stability... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs2501431 | CNR2 CNR2 rs2501431 | Synonymous coding variant in the cannabinoid receptor 2 gene that tags a hapl... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs3212227 | IL12B 3'UTR | IL12B 3'-UTR variant forming the canonical two-SNP psoriasis risk haplotype w... | Psoriasis & Spondyloarthropathy | Strong | |
| rs35829419 | NLRP3 Q705K | Gain-of-function missense variant in the NLRP3 inflammasome sensor that eleva... | Innate Immunity & Infection Defense | Moderate | |
| rs4810485 | CD40 | Intronic variant in CD40 regulating B-cell surface expression; the G allele d... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs660895 | HLA-DRB1 | Regulatory tag SNP in the HLA-DRB1 region; the G allele marks the HLA-DRB1*04... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs72613567 | HSD17B13 Splice Variant (;A) | Protective adenine insertion disrupting the HSD17B13 splice donor site, produ... | Liver Fat | Established | |
| rs12551268 | IL33 IL33 asthma-protective variant | Intronic IL33 variant where A-allele carriers showed a protective trend again... | Allergy & Atopic Disease | Emerging | |
| rs174575 | FADS2 | Intronic variant in FADS2 that reduces delta-6 desaturase activity, impairing... | Triglycerides & Fatty Acids | Strong | |
| rs1800947 | CRP +1059G>C | Synonymous exon 2 variant that influences baseline C-reactive protein express... | Vascular Inflammation & Remodeling | Strong | |
| rs2118181 | FBN1 | Intronic FBN1 variant associated with elevated thoracic aortic dissection ris... | Cardiomyopathy & Structural Heart | Emerging | |
| rs2298566 | SNX19 | Missense variant in sorting nexin 19 that alters endolysosomal positioning at... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs28940578 | MEFV M694I | Exon 10 missense variant in the inflammasome regulator pyrin, converting meth... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs3213094 | IL12B Promoter-region | Intronic IL12B variant in linkage with the promoter-regulatory haplotype; T a... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs3783550 | IL1A | Intronic variant within IL1A (Interleukin-1 alpha) associated with endometrio... | Endometriosis & Uterine Health | Moderate | |
| rs558269137 | FLG 2282del4 | Frameshift deletion eliminating filaggrin protein, the second most common Eur... | Skin & Eyes | Established | |
| rs6063 | FGG Gly191Arg | Rare missense variant in the fibrinogen gamma chain that disrupts fibrin poly... | Coagulation & Clotting Factors | Moderate | |
| rs6910071 | TSBP1 | MHC-region intronic variant tagging HLA-DRB1 shared epitope haplotypes; G all... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs12936231 | ORMDL3 ORMDL3 17q21 eQTL | Regulatory tagging SNP in the 17q21 asthma locus that is the strongest eQTL f... | Allergy & Atopic Disease | Strong | |
| rs174616 | FADS2 FADS2 Haplotype Block Variant | Intronic FADS2 variant tagging the FADS1/FADS2 haplotype block; A allele carr... | Triglycerides & Fatty Acids | Strong | |
| rs1800624 | AGER -374T/A | Promoter variant in the AGER gene that increases RAGE transcription approxima... | Hormones & Sleep | Moderate | |
| rs1800795 | IL6 -174G/C | Promoter variant controlling interleukin-6 expression — affects inflammation,... | Fitness & Body | Strong | |
| rs1831281 | CFH | Intronic CFH variant that tags the complement-risk haplotype; the C allele (c... | Vascular Inflammation & Remodeling | Moderate | |
| rs2069837 | IL6 | Intronic IL6 enhancer variant that regulates the anti-inflammatory gene GPNMB... | Longevity & Aging | Moderate | |
| rs28940579 | MEFV V726A | Exon 10 missense variant in the inflammasome regulator pyrin; one of five fou... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs2943634 | IRS1 | Intergenic variant near IRS1 at 2q36.3 associated with ischemic stroke risk, ... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs3087243 | CTLA4 CT60 | Immune checkpoint regulatory variant in the 3'UTR affecting T-cell activation... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs33980500 | TRAF3IP2 D10N | Missense variant in Act1 that abolishes IL-17 signaling by disrupting TRAF6 b... | Psoriasis & Spondyloarthropathy | Strong | |
| rs3758524 | LTBR LTBR regulatory variant | Intronic regulatory variant near the lymphotoxin beta receptor gene influenci... | Innate Immunity & Infection Defense | Emerging | |
| rs729302 | IRF5 | Near-gene variant tagging an IRF5 protective haplotype in the 5' promoter reg... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs12946510 | IKZF3 IKZF3 17q21 FOXO1-enhancer variant | Regulatory variant in a FOXO1-binding enhancer element flanking the IKZF3 gen... | Allergy & Atopic Disease | Strong | |
| rs1800625 | AGER AGER -429T>C | Promoter variant at position -429 in the AGER gene that increases RAGE transc... | Hormones & Sleep | Moderate | |
| rs1831282 | CFH | Intronic CFH variant at chromosome 1q31.3 associated with AMD risk; the C all... | Vascular Inflammation & Remodeling | Strong | |
| rs2153960 | FOXO3 | Intronic FOXO3 tag SNP whose A allele associates with higher circulating IGF-... | Longevity & Aging | Moderate | |
| rs28940580 | MEFV M680I | Exon 10 missense variant in the inflammasome regulator pyrin; one of five fou... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs30021 | SNX24 VEGFA Vascular Growth Co-variant | Intronic variant in SNX24 (sorting nexin 24) with roles in vascular endotheli... | Coronary Artery Disease & Atherosclerosis | Emerging | |
| rs3134883 | IL2RA | Intronic IL2RA variant independently associated with rheumatoid arthritis ris... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs3764880 | TLR8 A1G | X-linked initiator codon variant in TLR8 that fine-tunes the ratio of two TLR... | Innate Immunity & Infection Defense | Strong | |
| rs3805435 | TNIP1 | Intronic variant in the GPX3/TNIP1 regulatory locus on chromosome 5; the C al... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs4762326 | VEZT VEZT Endometriosis Cell Adhesion Variant | Intronic variant in VEZT (vezatin, adherens junction transmembrane protein) o... | Endometriosis & Uterine Health | Strong | |
| rs547154 | C2 IVS10 | Intronic C2 variant forming the H7 protective haplotype with CFB R32Q, reduci... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs61816761 | FLG R501X | Nonsense variant eliminating filaggrin protein, the major genetic risk factor... | Skin & Eyes | Established | |
| rs1295685 | IL13 | 3'-UTR regulatory variant in IL13 that influences IL-13 mRNA stability and ex... | Allergy & Atopic Disease | Moderate | |
| rs1927911 | TLR4 | Intronic TLR4 variant in the innate immune receptor gene; the A allele associ... | Vascular Inflammation & Remodeling | Moderate | |
| rs2301436 | FGFR1OP | Intronic variant in FGFR1OP (CEP43) at the RNASET2-FGFR1OP-CCR6 autoimmune su... | IBD & Mucosal Immunity | Strong | |
| rs3184504 | SH2B3 R262W | Pleiotropic missense variant reducing SH2B3 inhibitory function, increasing b... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs3743930 | MEFV E148Q | Exon 2 missense variant in the inflammasome regulator pyrin; the most common ... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs3774937 | NFKB1 NFKB1 promoter/regulatory variant | Intronic NFKB1 variant with genome-wide significant associations with ulcerat... | Innate Immunity & Infection Defense | Strong | |
| rs41298997 | IKBKE | Intronic variant in IKBKE (IKK-epsilon) associated with psoriasis susceptibil... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs55687265 | ATP8B4 ATP8B4 Phospholipid Flippase F436L | Missense variant in ATP8B4 converting phenylalanine to leucine at position 43... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs6837293 | PRKG2 | Intronic variant in PRKG2 (cGMP-dependent protein kinase II); the T allele wa... | Uric Acid & Kidney Function | Emerging | |
| rs7514229 | TNFSF4 TNFSF4 OX40 ligand variant | Intronic variant in TNFSF4 that tags an upstream regulatory haplotype associa... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs1295686 | IL13 IL-13 Atopy Promoter Variant | Intronic variant in IL13 that tags the atopic risk haplotype; the minor T all... | Allergy & Atopic Disease | Strong | |
| rs1414273 | CD58 | Intronic CD58 variant hosting the miR-548ac stem-loop; the C allele creates a... | Neurology & Cognition | Strong | |
| rs17300539 | ADIPOQ -11391G>A | Promoter variant affecting adiponectin secretion and metabolic syndrome risk | Fat Storage & Energy | Strong | |
| rs2253310 | FOXO3 | Intronic FOXO3 longevity variant; C allele (minor in East Asians) associated ... | Longevity & Aging | Moderate | |
| rs2631367 | SLC22A5 OCTN2 -207C>G | Promoter variant in SLC22A5 (OCTN2) that reduces carnitine transporter expres... | IBD & Mucosal Immunity | Strong | |
| rs340875 | PROX1 | Intronic variant in PROX1, the master transcription factor for lymphatic endo... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs35018800 | TYK2 TYK2 Ala928Val | A rare missense variant in the TYK2 pseudokinase (JH2) domain that partially ... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs3748067 | IL17A | 3'UTR variant in IL-17A that alters post-transcriptional regulation via miRNA... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs3775291 | TLR3 Leu412Phe | Missense variant in TLR3 that halves dsRNA-binding capacity, reducing antivir... | Innate Immunity & Infection Defense | Strong | |
| rs4349859 | HLA-B HLA-B27 proxy | Intronic tag SNP located 41 kb centromeric of HLA-B and 5.4 kb telomeric of M... | Psoriasis & Spondyloarthropathy | Established | |
| rs4848306 | IL1B | IL1B promoter -3737 G/A variant that modulates interleukin-1β expression; the... | Endometriosis & Uterine Health | Emerging | |
| rs641153 | CFB R32Q | Protective missense variant in complement factor B that reduces alternative p... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs7574865 | STAT4 Intron 3 | Intronic STAT4 variant that amplifies the interferon-alpha and IL-12 response... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs13408661 | IL1RL1 | Intronic variant in IL1RL1 (encoding the ST2 receptor for IL-33) tagging hapl... | Allergy & Atopic Disease | Moderate | |
| rs2274700 | CFH A473A | Synonymous CFH variant in complete LD with rs1410996 that tags the complement... | Longevity & Aging | Strong | |
| rs28929474 | SERPINA1 Z allele (E342K) | Most common alpha-1 antitrypsin deficiency variant causing protein misfolding... | Metabolic Enzymes & Rare Disorders | Established | |
| rs3761847 | TRAF1 | Intronic GWAS variant in the TRAF1-C5 locus on chromosome 9 robustly associat... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs3796508 | TLR6 Val327Met | Missense variant substituting valine with methionine at position 327 of TLR6,... | Innate Immunity & Infection Defense | Emerging | |
| rs4406273 | HLA-C | Near-HLA-C intergenic variant that tags HLA-C*06:02 haplotype, conferring ris... | Psoriasis & Spondyloarthropathy | Strong | |
| rs6445975 | PXK | Intronic PXK variant; the G allele is a replicated GWAS risk allele for syste... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs1342326 | IL33 IL33 regulatory variant | Regulatory variant upstream of IL33; the C allele elevates IL-33 expression, ... | Allergy & Atopic Disease | Strong | |
| rs3790565 | IL12RB2 | Intronic IL12RB2 variant associated with IL-12 signaling pathway variation an... | IBD & Mucosal Immunity | Moderate | |
| rs3804099 | TLR2 | Synonymous variant in Toll-Like Receptor 2 affecting mRNA stability and splic... | Innate Immunity & Infection Defense | Moderate | |
| rs3816769 | STAT3 STAT3 co-variant | Intronic STAT3 variant where the T allele (reference, ~66%) increases risk fo... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs3825942 | LOXL1 G153D (Gly153Asp) | Missense variant in the elastin-crosslinking enzyme LOXL1; the common G allel... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs41295061 | IL2RA | Regulatory variant in the IL2RA locus altering LEF1 transcription factor bind... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs519664 | TTC39B TTC39B rs519664 | Intronic variant in TTC39B (9p22) that increases endometriosis susceptibility... | Endometriosis & Uterine Health | Strong | |
| rs582757 | TNFAIP3 TNFAIP3 A20 regulatory variant | Intronic regulatory variant in TNFAIP3 — the primary NF-kB brake gene — with ... | Psoriasis & Spondyloarthropathy | Strong | |
| rs7151526 | SERPINA1 | Regulatory variant downstream of SERPINA1 associated with increased susceptib... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs9268839 | HLA-DRA | Intergenic tag SNP upstream of HLA-DRA; the G allele is the primary GWAS sign... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs13424006 | IL1RL1 | Intronic IL1RL1 variant in the 10th intron of the ST2 receptor gene; C allele... | Allergy & Atopic Disease | Moderate | |
| rs3850641 | TNFSF4 TNFSF4 (OX40L) Intron 1 Variant | Intronic variant in TNFSF4 (OX40 ligand) linked to a promoter haplotype that ... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs3890745 | MMEL1 MMEL1 rs3890745 | Intronic variant near MMEL1 and TNFRSF14 on chromosome 1p36; the C allele is ... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs559406 | PTPN2 | Intronic PTPN2 variant whose G allele reduces T-cell protein tyrosine phospha... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs610604 | TNFAIP3 | Intronic variant in TNFAIP3 whose G allele is the primary psoriasis susceptib... | Psoriasis & Spondyloarthropathy | Strong | |
| rs1420101 | IL1RL1 | Intronic regulatory variant in IL1RL1 that lowers soluble ST2 (sST2) decoy re... | Allergy & Atopic Disease | Strong | |
| rs2104772 | TNC | Affects tenascin C protein levels and elasticity, influencing tendon injury r... | Fitness & Body | Strong | |
| rs2536 | MTOR | 3'UTR variant that alters miR-150 binding affinity; the C allele increases mi... | Longevity & Aging | Moderate | |
| rs3918242 | MMP9 MMP9 C-1562T | Promoter variant that disrupts an SP1 transcription factor binding site, incr... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs4845625 | IL6R | Intronic IL6R variant associated with coronary artery disease risk, elevated ... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs5742909 | CTLA4 Promoter -318C/T | Promoter variant that increases CTLA-4 transcription; T allele carriers show ... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs61751629 | CARD14 Glu422Lys | Rare missense variant in the keratinocyte NF-κB scaffold protein CARD14 that ... | Psoriasis & Spondyloarthropathy | Emerging | |
| rs6542095 | IL1A IL1A rs6542095 | Regulatory variant near the IL1A (Interleukin-1 alpha) gene associated with m... | Endometriosis & Uterine Health | Moderate | |
| rs7528684 | FCRL3 -169C>T | Promoter variant in FCRL3 that alters NF-κB binding and elevates FCRL3 expres... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs146527530 | CTSS CTSS AD Risk Signal (Budu-Aggrey 2023) | Third independent CTSS-locus atopic dermatitis risk signal from the Budu-Aggr... | Allergy & Atopic Disease | Moderate | |
| rs1718119 | P2RX7 Ala348Thr | Gain-of-function variant in the P2X7 receptor that increases ATP-gated pore f... | Neurology & Cognition | Moderate | |
| rs182052 | ADIPOQ ADIPOQ promoter -10066A>G | Intronic/promoter-region ADIPOQ variant where the A allele reduces circulatin... | Fat Storage & Energy | Strong | |
| rs4252130 | PLG PLG promoter/intronic variant | Intronic PLG variant tagging a regional haplotype that reduces plasminogen ex... | Innate Immunity & Infection Defense | Moderate | |
| rs4537545 | IL6R IL6R intron variant | Intronic IL6R variant in linkage disequilibrium with the functional Asp358Ala... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs4562997 | SMAD3 | Second intronic enhancer variant in SMAD3 that modulates TGF-beta effector si... | IBD & Mucosal Immunity | Moderate | |
| rs5029937 | TNFAIP3 | Intronic risk variant within TNFAIP3 intron 2 that independently increases su... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs6887695 | IL12B Upstream regulatory | Upstream regulatory variant ~60 kb 5' of IL12B, forming the canonical two-SNP... | Psoriasis & Spondyloarthropathy | Strong | |
| rs7234029 | PTPN2 | Intronic PTPN2 variant that reduces expression of T-cell protein tyrosine pho... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs7951 | C3 | Synonymous C3 variant associated with reduced serum complement C3 levels and ... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs146597587 | IL33 | Rare splice acceptor variant that abolishes IL-33/ST2 signalling; the C allel... | Allergy & Atopic Disease | Strong | |
| rs1862513 | RETN -420C>G | Promoter variant that increases resistin expression via Sp1/Sp3 transcription... | Fat Storage & Energy | Moderate | |
| rs2236212 | ELOVL2 | Intronic variant in ELOVL2 that reduces elongase-2 enzyme activity, impairing... | Triglycerides & Fatty Acids | Moderate | |
| rs2672598 | HTRA1 | Promoter variant at -487 in HTRA1 that elevates HTRA1 serine protease express... | Longevity & Aging | Strong | |
| rs4252185 | PLG | Intronic PLG variant (intron 1) whose C allele is enriched in Europeans and a... | Innate Immunity & Infection Defense | Emerging | |
| rs4888378 | CFDP1 | Intronic CFDP1 locus variant that regulates BCAR1 expression in vascular tiss... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs5029939 | TNFAIP3 | Intronic variant near TNFAIP3 that tags a 6q23 haplotype strongly associated ... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs6757908 | EIF2AK3-AS1 | Rare intronic variant in EIF2AK3-AS1, an antisense long non-coding RNA that r... | Endometriosis & Uterine Health | Emerging | |
| rs7152376 | NFKBIA | Regulatory variant upstream of NFKBIA that specifically elevates risk of psor... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs841 | GCH1 | Intronic/3'UTR GCH1 variant tagging reduced tetrahydrobiopterin (BH4) synthes... | Blood Pressure & Hypertension | Moderate | |
| rs9332736 | C2 28bp deletion (type I C2 deficiency) | Frameshift deletion in C2 exon 6 causing complete complement C2 deficiency, i... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs167769 | STAT6 | Intronic variant in STAT6 (intron 2) that forms a functional haplotype with r... | Allergy & Atopic Disease | Strong | |
| rs243865 | MMP2 C-1306T | Promoter polymorphism that disrupts an Sp1-binding site and reduces MMP-2 enz... | Fitness & Body | Moderate | |
| rs3091244 | CRP -286C>T>A | Triallelic promoter variant that strongly influences basal CRP transcription;... | Vascular Inflammation & Remodeling | Strong | |
| rs4648127 | NFKB1 NFKB1 intronic variant | Rare protective intronic variant in the master immune transcription factor NF... | Innate Immunity & Infection Defense | Moderate | |
| rs4958847 | IRGM | Intronic IRGM variant that impairs autophagy-mediated clearance of intracellu... | IBD & Mucosal Immunity | Strong | |
| rs61752717 | MEFV M694V | The most common and clinically severe MEFV mutation, converting methionine to... | TNF, NF-kB & Inflammatory Cytokines | Established | |
| rs72634030 | RABEP1 | Intronic RABEP1 variant associated with rheumatoid arthritis risk, acting thr... | Autoimmune Tolerance & T-Cell Regulation | Emerging | |
| rs9332739 | C2 E318D | Missense variant in complement component C2 forming a protective haplotype wi... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs16947078 | TBX21 TBX21 T-bet asthma variant | Intergenic regulatory variant near TBX21 associated with allergic asthma susc... | Allergy & Atopic Disease | Strong | |
| rs2524299 | FADS2 | Intronic regulatory variant in FADS2 (Block 2 haplotype) that reduces basal F... | Triglycerides & Fatty Acids | Moderate | |
| rs2764264 | FOXO3 | Intronic FOXO3 variant that disrupts an NKX3 transcription factor binding sit... | Longevity & Aging | Strong | |
| rs3093059 | CRP -757T>C | Promoter variant that elevates baseline C-reactive protein levels, increasing... | Vascular Inflammation & Remodeling | Strong | |
| rs4696480 | TLR2 T-16934A | Promoter variant in Toll-Like Receptor 2 that increases TLR2 expression, asso... | Innate Immunity & Infection Defense | Moderate | |
| rs501120 | CXCL12 | Regulatory variant ~80 kb downstream of CXCL12 (SDF-1) associated with elevat... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs61753993 | VWF D141G | Missense variant in von Willebrand factor (p.Asp141Gly) associated with type ... | Von Willebrand & Anticoagulant Proteins | Moderate | |
| rs6920220 | TNFAIP3 | Regulatory variant upstream of TNFAIP3 that reduces A20 expression and impair... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs7746808 | IL23A | Intergenic variant near the IL23A locus associated with psoriasis and psoriat... | Psoriasis & Spondyloarthropathy | Emerging | |
| rs17250932 | TBX21 TBX21 Promoter Variant | Upstream promoter variant in TBX21 that reduces neonatal IL-5 and IL-13 secre... | Allergy & Atopic Disease | Emerging | |
| rs2779249 | NOS2 Promoter -1026C/A | Functional promoter variant that increases iNOS transcriptional activity up t... | Longevity & Aging | Moderate | |
| rs4073 | IL8 -251A>T | Promoter variant affecting interleukin-8 transcription and inflammatory burden | Vascular Inflammation & Remodeling | Strong | |
| rs4833095 | TLR1 N248S | Missense variant replacing asparagine with serine at TLR1 position 248 in the... | Innate Immunity & Infection Defense | Strong | |
| rs505922 | ABO ABO blood group tag SNP | Tag SNP for the ABO blood group locus; T allele marks blood type O (lower clo... | Coronary Artery Disease & Atherosclerosis | Established | |
| rs6693831 | IL23R | Intronic IL23R variant where the minor T allele is associated with increased ... | IBD & Mucosal Immunity | Moderate | |
| rs763780 | IL17F His161Arg | Missense variant that reduces IL-17F bioactivity and acts as a natural IL-17F... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs17293632 | SMAD3 | Intronic regulatory variant in SMAD3 that alters TGF-beta effector signaling ... | Allergy & Atopic Disease | Strong | |
| rs2802292 | FOXO3 | Longevity-associated intronic enhancer variant with 1.9-fold increased probab... | Longevity & Aging | Established | |
| rs3025058 | MMP3 5A/6A | Promoter polymorphism affecting MMP3 enzyme expression levels, influencing ca... | Fitness & Body | Strong | |
| rs4729189 | PON2 | Intronic PON2 variant associated with variation in serum paraoxonase activity... | Vascular Inflammation & Remodeling | Emerging | |
| rs4986790 | TLR4 Asp299Gly | Missense variant in Toll-like receptor 4 reducing bacterial endotoxin recogni... | Innate Immunity & Infection Defense | Strong | |
| rs56062135 | SMAD3 SMAD3 intronic variant | Intronic SMAD3 variant tagging the CAD-protective haplotype where the T allel... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs689466 | PTGS2 A-1195G | Promoter variant in the PTGS2/COX-2 gene that reduces baseline COX-2 expressi... | IBD & Mucosal Immunity | Moderate | |
| rs6947337 | INHBA | Activin A signaling variant near INHBA linking adipocyte dysfunction to share... | Appetite & Obesity | Moderate | |
| rs7753394 | TNFAIP3 | Intergenic tag SNP in the 6q23 regulatory region upstream of TNFAIP3 that co-... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs17612852 | HLA-DQA1 HLA-DQA1 Peanut Allergy Tag SNP | Intronic tag SNP in HLA-DQA1 in strong LD with HLA-DQA1*01:02; the G allele i... | Allergy & Atopic Disease | Strong | |
| rs2811712 | CDKN2BAS | Regulatory variant in the ANRIL long non-coding RNA at the 9p21.3 locus that ... | Longevity & Aging | Moderate | |
| rs4986791 | TLR4 Thr399Ile | Missense variant in Toll-like receptor 4 that co-segregates with Asp299Gly on... | Innate Immunity & Infection Defense | Strong | |
| rs6908425 | CDKAL1 | Intronic variant in CDKAL1, a tRNA methylthiotransferase gene; the C allele i... | IBD & Mucosal Immunity | Strong | |
| rs9807989 | IL18R1 | Upstream regulatory variant of IL18R1 on chromosome 2q12; the T risk allele i... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs17699436 | TBX21 TBX21 Downstream Regulatory Variant | Intergenic variant 5 kb downstream of TBX21 (encoding the T-bet transcription... | Allergy & Atopic Disease | Moderate | |
| rs1800693 | TNFRSF1A | Splice-region variant in TNFR1 that generates a soluble Δ6 isoform mimicking ... | Neurology & Cognition | Strong | |
| rs1801181 | CBS A360A | A synonymous variant in CBS affecting homocysteine metabolism and associated ... | Methylation & Detox | Moderate | |
| rs5743618 | TLR1 I602S | Coding variant replacing isoleucine with serine at TLR1 position 602, disrupt... | Innate Immunity & Infection Defense | Strong | |
| rs619203 | ROS1 Ser2229Cys | Missense variant in the ROS1 receptor tyrosine kinase associated with atherot... | Coronary Artery Disease & Atherosclerosis | Emerging | |
| rs867186 | PROCR S219G | Missense variant in the endothelial protein C receptor gene that increases EP... | Von Willebrand & Anticoagulant Proteins | Strong | |
| rs1800925 | IL13 -1112C>T | Promoter variant that selectively increases IL-13 expression in Th2 lymphocyt... | Allergy & Atopic Disease | Strong | |
| rs266729 | ADIPOQ -11391G>C | Promoter variant reducing adiponectin transcription, increasing T2D, NAFLD, a... | Fat Storage & Energy | Strong | |
| rs5743708 | TLR2 R753Q | Missense variant in Toll-Like Receptor 2 impairing innate immune signaling to... | Innate Immunity & Infection Defense | Strong | |
| rs6797312 | SERPINI1 | Intronic variant in the neuroserpin gene; the A allele has been associated wi... | Coronary Artery Disease & Atherosclerosis | Emerging | |
| rs7030781 | VEGFA VEGFA Regulatory Co-variant | Chromosome 9 regulatory co-variant near a lncRNA locus that co-segregates wit... | Vascular Inflammation & Remodeling | Emerging | |
| rs7517847 | IL23R | Intronic IL23R variant in which the T allele increases susceptibility to Croh... | IBD & Mucosal Immunity | Strong | |
| rs1801275 | IL4R Q576R | Gain-of-function missense variant in the IL-4 receptor alpha chain that ampli... | Allergy & Atopic Disease | Strong | |
| rs5743810 | TLR6 Ser249Pro | Coding variant replacing serine with proline at TLR6 position 249, altering T... | Innate Immunity & Infection Defense | Moderate | |
| rs7530511 | IL23R Leu310Pro | Missense variant in the IL-23 receptor that substitutes leucine for proline a... | IBD & Mucosal Immunity | Moderate | |
| rs1805010 | IL4R Ile75Val | Missense variant in the extracellular domain of the IL-4 receptor alpha chain... | Allergy & Atopic Disease | Moderate | |
| rs350845 | SIRT6 | Intronic eQTL in SIRT6 where the rare A allele upregulates SIRT6 expression a... | Longevity & Aging | Moderate | |
| rs5743836 | TLR9 Promoter -1237T/C | TLR9 promoter variant that creates an IL-6-responsive element and estrogen-se... | Innate Immunity & Infection Defense | Moderate | |
| rs60910145 | APOL1 G1 I384M | Second component of the APOL1 G1 kidney disease risk haplotype — a missense v... | Cholesterol & Lipoproteins | Established | |
| rs700651 | BOLL | Intronic variant near the BOLL gene associated with increased intracranial an... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs1805011 | IL4R IL4R Glu375Ala | Missense variant in the extracellular domain of the IL-4 receptor alpha chain... | Allergy & Atopic Disease | Moderate | |
| rs7025486 | DAB2IP DAB2IP intron variant | Intronic variant in DAB2IP associated with increased risk of abdominal aortic... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs1837253 | TSLP Upstream Variant | Upstream regulatory variant in TSLP reducing cytokine expression; the protect... | Allergy & Atopic Disease | Strong | |
| rs28362944 | SERPING1 | 5' UTR variant in C1-inhibitor gene that promotes partial exon 2 skipping, re... | Hormones & Sleep | Moderate | |
| rs3803304 | AKT1 | Intronic AKT1 variant near a conserved exon-intron boundary; the G allele is ... | Longevity & Aging | Moderate | |
| rs187080438 | CTSS Cathepsin S antigen presentation variant | Intronic variant in the CTSS locus associated with elevated atopic dermatitis... | Allergy & Atopic Disease | Moderate | |
| rs1979277 | SHMT1 C1420T | Alters one-carbon metabolism and folate distribution; influences cancer risk,... | Methylation & Detox | Moderate | |
| rs4946935 | FOXO3 | Functionally validated FOXO3 intronic variant that creates an SRF binding sit... | Longevity & Aging | Strong | |
| rs7091565 | ANXA11 ANXA11 rs7091565 | 3' UTR variant in ANXA11 (annexin A11) in strong LD with the functional R230C... | Innate Immunity & Infection Defense | Moderate | |
| rs2230912 | P2RX7 Gln460Arg | Missense variant in the C-terminal domain of the P2X7 receptor that disrupts ... | Neurology & Cognition | Moderate | |
| rs34536443 | TYK2 TYK2 p.Pro1104Ala | A missense variant in TYK2 that partially impairs JAK-family signaling downst... | Hormones & Sleep | Strong | |
| rs767603 | LOC105378189 | Regulatory variant near LOC105378189 non-coding RNA locus on chromosome 14q23... | Coronary Artery Disease & Atherosclerosis | Moderate | |
| rs9298506 | SOX17 | Regulatory tag variant near SOX17 at chromosome 8q11.23 associated with intra... | Vascular Inflammation & Remodeling | Strong | |
| rs1898671 | TSLP TSLP Intronic Variant (Atopic Dermatitis) | Intronic TSLP variant that modulates thymic stromal lymphopoietin activity, w... | Allergy & Atopic Disease | Moderate | |
| rs551397 | CFH | Intronic CFH variant that tags the AMD-risk haplotype; the C allele tracks co... | Longevity & Aging | Moderate | |
| rs7664413 | VEGFC | Intronic variant in the primary lymphangiogenesis growth factor gene associat... | Innate Immunity & Infection Defense | Emerging | |
| rs1950897 | RAD51B RAD51B Intronic RA Susceptibility Variant | Intronic variant in RAD51B on chromosome 14; the T allele is associated with ... | Allergy & Atopic Disease | Strong | |
| rs2300747 | CD58 | Intronic variant in CD58 (LFA-3) that modulates T-cell costimulation and Treg... | Neurology & Cognition | Strong | |
| rs8177374 | TIRAP Ser180Leu | Missense variant in the TLR2/TLR4 adaptor protein Mal that modulates innate i... | Innate Immunity & Infection Defense | Strong | |
| rs9818870 | MRAS | 3' UTR variant near miRNA binding sites in MRAS, associated with ~15% increas... | Coronary Artery Disease & Atherosclerosis | Strong | |
| rs2040410 | HLA-DQA1 HLA-DQ Autoimmune Tag SNP | Intronic tag SNP near HLA-DQA1 that marks the DR3 (DRB1*0301-DQA1*0501-DQB1*0... | Allergy & Atopic Disease | Strong | |
| rs2040704 | RAD50 RAD50/IL13 5q31 Atopic March Locus | Intronic variant in the RAD50/TH2LCRR region at 5q31.1 that tags an enhancer ... | Allergy & Atopic Disease | Moderate | |
| rs20541 | IL13 R130Q | Missense variant in IL-13 that enhances Th2 cytokine signaling, elevating ser... | Allergy & Atopic Disease | Strong | |
| rs2069705 | IFNG IFNG Promoter -1616C/T | Upstream regulatory variant ~1,616 bp before the IFNG transcription start sit... | Allergy & Atopic Disease | Moderate | |
| rs3816183 | HAAO Ile37Val | Missense variant in the kynurenine pathway enzyme HAAO that shifts tryptophan... | Hormones & Sleep | Moderate | |
| rs2070874 | IL4 IL4 C-33T | 5'-UTR variant 33 bases downstream of the IL-4 transcription start site; the ... | Allergy & Atopic Disease | Strong | |
| rs2158177 | TH2LCRR RAD50/IL13 Region Variant | Intronic variant in TH2LCRR, a long noncoding RNA residing in the 5q31.1 RAD5... | Allergy & Atopic Disease | Moderate | |
| rs2227284 | IL4 IL4 T+2979G | Intronic regulatory variant in IL-4, the master Th2 cytokine; the T allele im... | Allergy & Atopic Disease | Moderate | |
| rs2228145 | IL6R Asp358Ala | Missense variant in the IL-6 receptor that increases receptor shedding and en... | Allergy & Atopic Disease | Strong | |
| rs2240032 | RAD50 RAD50 RHS7 TH2-LCR Variant | Intronic RAD50 variant in the Th2 locus control region (RHS7); T allele alter... | Allergy & Atopic Disease | Moderate | |
| rs6954668 | SFRP5 SFRP5 Wnt5a inhibitor variant | Intergenic variant near the SFRP5 adipokine locus; the A allele is strongly e... | Fat Storage & Energy | Emerging | |
| rs2243250 | IL4 IL4 -589C>T | Promoter polymorphism 589 bases upstream of the IL-4 transcription start site... | Allergy & Atopic Disease | Strong | |
| rs9470080 | FKBP5 | Intronic FKBP5 variant in the stress-aging haplotype block — T allele carrier... | Longevity & Aging | Strong | |
| rs2243290 | IL4 IL4 Intron 3 Protective Haplotype Variant | Intronic IL4 variant that forms part of the protective C-G-C haplotype (rs224... | Allergy & Atopic Disease | Moderate | |
| rs4926 | SERPING1 Val480Met | Missense variant in C1-inhibitor gene associated with insomnia risk through n... | Hormones & Sleep | Moderate | |
| rs2244012 | RAD50 RAD50 Intron 2 Variant | Intronic variant in RAD50 on chromosome 5q31.1 that was the top GWAS hit for ... | Allergy & Atopic Disease | Moderate | |
| rs2297839 | CHI3L1 CHI3L1 Intron Variant | Intronic variant in CHI3L1 associated with circulating YKL-40 levels and modu... | Allergy & Atopic Disease | Emerging | |
| rs2303065 | SPINK5 SPINK5 His396His (c.1188T>C) | Synonymous variant in SPINK5 exon 13 that tags the same risk haplotype as the... | Allergy & Atopic Disease | Moderate | |
| rs2303067 | SPINK5 SPINK5 Lys420Glu | Missense variant in SPINK5 encoding LEKTI domain 6 (p.Lys420Glu) that increas... | Allergy & Atopic Disease | Moderate | |
| rs2305480 | GSDMB GSDMB Pro311Ser protective haplotype | Missense variant in gasdermin B that increases GSDMB expression and pyroptoti... | Allergy & Atopic Disease | Strong | |
| rs3751143 | P2RX7 Glu496Ala | Loss-of-function variant in the P2X7 receptor that reduces inflammatory respo... | Neurology & Cognition | Strong | |
| rs2602899 | ADH5 ADH5 Promoter NF-kB Variant | Regulatory SNP in the ADH5 promoter at a potential NF-kB binding site; the pr... | Allergy & Atopic Disease | Moderate | |
| rs968567 | FADS2 FADS2 Promoter D6D Activity Variant | Promoter variant in FADS2 that increases delta-6 desaturase (D6D) expression ... | Triglycerides & Fatty Acids | Moderate | |
| rs2851301 | ADH5 ADH5 Second NF-kB Site Variant | Upstream promoter variant in ADH5 at a potential NF-kB binding site; the mino... | Allergy & Atopic Disease | Emerging | |
| rs2872507 | IKZF3 | 17q21 regulatory variant in the IKZF3-ORMDL3-GSDMB locus with opposite effect... | Allergy & Atopic Disease | Strong | |
| rs4684059 | HRH1 | Intronic variant in the histamine H1 receptor gene associated with altered re... | Methylation & Detox | Emerging | |
| rs99780 | FADS2 | Intronic variant in the FADS1-FADS2 cluster influencing delta-6 desaturase ac... | Triglycerides & Fatty Acids | Moderate | |
| rs28730619 | ADH5 | Intronic variant in ADH5 (GSNOR) associated with elevated childhood asthma ri... | Allergy & Atopic Disease | Moderate | |
| rs2967677 | CERS4 Ceramide synthase 4 locus variant | A 3'UTR variant in the CERS4/NFILZ locus on chromosome 19 associated with ato... | Allergy & Atopic Disease | Strong | |
| rs4149584 | TNFRSF1A R92Q | Missense variant in TNF receptor 1 that causes low-penetrance TRAPS (recurren... | Neurology & Cognition | Strong | |
| rs3024971 | STAT6 | Intronic variant in STAT6 near the 3' end of the gene that modulates STAT6 mR... | Allergy & Atopic Disease | Moderate | |
| rs4803217 | IFNL3 3'UTR | 3' untranslated region variant in IFNL3 (IL28B) that controls mRNA stability ... | Pharmacogenomics | Strong | |
| rs324011 | STAT6 | Intronic variant in STAT6 (intron 2) that creates an NF-κB binding site, incr... | Allergy & Atopic Disease | Strong | |
| rs324013 | STAT6 | Promoter variant in STAT6 that alters transcription factor binding; the T all... | Allergy & Atopic Disease | Moderate | |
| rs653178 | SH2B3 ATXN2/SH2B3 12q24 pleiotropic locus | Pleiotropic 12q24 locus variant in SH2B3 (LNK) modulating JAK-STAT cytokine s... | Blood Sugar & Diabetes | Strong | |
| rs78534766 | ADCY7 ADCY7 D439E | Low-frequency missense variant in adenylyl cyclase 7 that reduces cAMP synthe... | Hormones & Sleep | Strong | |
| rs35699176 | ZNF77 ZNF77 Q100* | Nonsense variant truncating ZNF77 at codon 100, impairing bronchial epithelia... | Allergy & Atopic Disease | Emerging | |
| rs3771166 | IL1RL1/IL18R1 | GABRIEL Consortium lead GWAS SNP at the IL1RL1/IL18R1 locus on chromosome 2q1... | Allergy & Atopic Disease | Strong | |
| rs3771175 | IL1RL1 IL1RL1 receptor variant | A 3'-UTR variant in IL1RL1 (the ST2 receptor gene); the A allele increases ST... | Allergy & Atopic Disease | Moderate | |
| rs819147 | AHCY | Regulatory variant affecting S-adenosylhomocysteine hydrolase expression, inf... | Methylation & Detox | Moderate | |
| rs3806933 | TSLP | Functional promoter variant in TSLP that creates an AP-1 transcription factor... | Allergy & Atopic Disease | Moderate | |
| rs3939286 | IL33 IL33 intronic asthma variant | Regulatory variant ~5 kb upstream of IL33; the T allele is associated with in... | Allergy & Atopic Disease | Strong | |
| rs4129267 | IL6R IL6R intronic multi-trait variant | Intronic IL6R variant in perfect linkage disequilibrium with the functional A... | Allergy & Atopic Disease | Strong | |
| rs4794067 | TBX21 TBX21 T-bet Promoter -1993T>C | Promoter variant ~1993 bp upstream of TBX21 (encoding the T-bet master transc... | Allergy & Atopic Disease | Moderate | |
| rs4950928 | CHI3L1 YKL-40 Promoter Variant (-131C>G) | Promoter variant controlling YKL-40 (chitinase 3-like 1) expression; the comm... | Allergy & Atopic Disease | Strong | |
| rs6062486 | RTEL1 Telomere helicase immune variant | Intronic variant in RTEL1 (regulator of telomere elongation helicase 1) assoc... | Allergy & Atopic Disease | Strong | |
| rs61816766 | FLG Filaggrin second variant | Intronic FLG-locus variant strongly associated with atopic dermatitis — the C... | Allergy & Atopic Disease | Strong | |
| rs6589702 | PRG2 PRG2 Eosinophil Major Basic Protein Variant | Intergenic regulatory variant near the PRG2/PRG3 eosinophil granule protein c... | Allergy & Atopic Disease | Emerging | |
| rs7125552 | EMSY EMSY Haplotype Partner Allergy Variant | Intronic EMSY variant that defines the high-risk haplotype at 11q13.5; the G ... | Allergy & Atopic Disease | Moderate | |
| rs7130588 | LRRC32 | Regulatory variant near LRRC32 (GARP) on chromosome 11q13.5; the G allele inc... | Allergy & Atopic Disease | Strong | |
| rs71625130 | SNX27 1q21.3 T-cell signaling / Th17 locus variant | Intronic SNX27 variant at the 1q21.3 GWAS locus that increases atopic dermati... | Allergy & Atopic Disease | Strong | |
| rs7192 | HLA-DRA HLA-DRA Leu242Val | Missense variant (Leu242Val) in the HLA-DRA alpha chain; the T allele tags HL... | Allergy & Atopic Disease | Strong | |
| rs7216389 | GSDMB ORMDL3 17q21 asthma risk | Intronic GSDMB variant that acts as an eQTL for ORMDL3; the T allele elevates... | Allergy & Atopic Disease | Established | |
| rs72823628 | IL1RL1 | Intronic variant in the IL1RL1/IL18R1 receptor gene cluster on chromosome 2q1... | Allergy & Atopic Disease | Moderate | |
| rs7927894 | EMSY | Regulatory variant near the EMSY/C11orf30 locus; T allele increases EMSY expr... | Allergy & Atopic Disease | Strong | |
| rs7927997 | EMSY EMSY/C11orf30 Atopy Regulatory Variant | Regulatory variant near C11orf30 (EMSY) on chromosome 11q13.5; the T allele r... | Allergy & Atopic Disease | Strong | |
| rs8111930 | MRPL4 MRPL4 Atopy-Associated Intronic Variant | Intronic variant in MRPL4 on chromosome 19p13.2 that alters transcription fac... | Allergy & Atopic Disease | Moderate | |
| rs6897932 | IL7R T244I | Splicing variant in the IL-7 receptor alpha chain that shifts the balance tow... | Neurology & Cognition | Strong | |
| rs872129 | CHI3L1 CHI3L1 eQTL Variant | Third independent eQTL signal at the CHI3L1/YKL-40 locus on chromosome 1q32.1... | Allergy & Atopic Disease | Moderate | |
| rs8832 | IL4R IL4R 3'UTR Asthma Exacerbation Variant | 3' untranslated region variant in the IL-4 receptor alpha chain gene; the G a... | Allergy & Atopic Disease | Moderate | |
| rs907091 | IKZF3 IKZF3 miRNA Binding Region Variant | A 3'UTR variant in IKZF3 that alters miR-326 binding affinity, reducing Aiolo... | Allergy & Atopic Disease | Moderate | |
| rs911263 | RAD51B RAD51B RA Proxy Variant | Intronic proxy variant in RAD51B associated with seropositive rheumatoid arth... | Allergy & Atopic Disease | Moderate | |
| rs8099917 | IFNL3 | Intergenic variant upstream of IFNL3 — second major IL28B locus predictor of ... | Pharmacogenomics | Established | |
| rs9275596 | HLA-DQ HLA-DQ Region Peanut Allergy Locus | Intergenic tag SNP between HLA-DQB1 and HLA-DQA2 tagging the HLA-DQA1*01:02 r... | Allergy & Atopic Disease | Strong | |
| rs950881 | IL1RL1 IL1RL1 intronic variant | Intronic variant in the IL1RL1 gene on chromosome 2q12 encoding the ST2 recep... | Allergy & Atopic Disease | Moderate | |
| rs963917 | RAD51B RAD51B Central European RA Variant | A 3' UTR variant in RAD51B that alters miRNA-616 binding efficiency and is as... | Allergy & Atopic Disease | Emerging | |
| rs992969 | IL33 | Regulatory variant upstream of IL33 encoding interleukin-33; the A allele inc... | Allergy & Atopic Disease | Strong | |
| rs7958311 | P2RX7 Arg270His | P2RX7 variant with a unique dual mechanism — gain-of-function in channel open... | Neurology & Cognition | Moderate |