Research
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