Tag
Autoimmune
288 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs1000940 | RABEP1 RABEP1 Metabolic-Immune Regulatory Variant | Intronic variant in RABEP1 associated with fasting glucose modulation under p... | Autoimmune Tolerance & T-Cell Regulation | Emerging | |
| 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 | |
| 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 | |
| rs10499194 | TNFAIP3 | Intergenic regulatory variant at 6q23 near TNFAIP3 whose T allele is protecti... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs10516487 | BANK1 R61H | BANK1 scaffold protein missense variant that shifts B-cell receptor signaling... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs10050860 | ERAP1 D575N | Missense variant (Asp575Asn) in the ERAP1 catalytic domain that modestly redu... | Psoriasis & Spondyloarthropathy | Strong | |
| rs10488631 | IRF5 | Near-gene regulatory variant tagging an IRF5 haplotype that elevates interfer... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs104895431 | NOD2 | Rare NOD2 missense variant (Ser431Leu) that reduces NF-κB activation in respo... | IBD & Mucosal Immunity | Strong | |
| 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 | |
| rs1016140 | CD58 | Intronic CD58 variant with a dual role — the G allele increases T-cell activi... | Neurology & Cognition | Moderate | |
| rs104895444 | NOD2 | Rare NOD2 missense variant (Val793Met) identified in IBD deep-resequencing; c... | IBD & Mucosal Immunity | Moderate | |
| rs1064793917 | SERPING1 | Frameshift deletion in SERPING1 (p.Lys390fs) abolishing C1-inhibitor producti... | B-Cell Immunity & Antibody-Mediated Disease | Established | |
| rs10794648 | IFNLR1/GRHL3 | Intergenic regulatory variant near IFNLR1 that contacts GRHL3 via chromatin l... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| 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 | |
| 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 | |
| rs1050152 | SLC22A4 OCTN1 L503F | Missense variant in SLC22A4 encoding the organic cation/ergothioneine transpo... | Allergy & Atopic Disease | Strong | |
| rs10800309 | FCGR2A FCGR2A intronic variant | Intronic upstream variant in FCGR2A that modulates surface expression of the ... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs12101261 | TSHR TSHR Intron 1 Adjacent Regulatory Variant | Intronic regulatory variant in TSHR intron 1 that is the primary PLZF repress... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs10489629 | IL23R | Intronic IL23R variant in LD block 2 where the T allele is associated with in... | IBD & Mucosal Immunity | 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 | |
| rs1217414 | PTPN22 | Intronic PTPN22 variant independently associated with psoriasis and ankylosin... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs12191877 | HLA-C Tag for *06:02 | Tag SNP for HLA-C*06:02, the strongest genetic risk factor for psoriasis, det... | Psoriasis & Spondyloarthropathy | Established | |
| rs10849448 | LTBR | Regulatory variant in the lymphotoxin beta receptor gene associated with incr... | Innate Immunity & Infection Defense | Strong | |
| rs1234314 | TNFSF4 | Intronic variant in TNFSF4 that reduces OX40 ligand promoter activity and is ... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| 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 | |
| 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 | |
| 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 | |
| rs13277113 | BLK | Regulatory variant upstream of BLK that reduces B-lymphoid tyrosine kinase ex... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs17561 | IL1A Ala114Ser | Missense variant in IL-1α (Ala114Ser) that acts as a common hypomorphic mutat... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs1058932 | CYP2C8 | CYP2C8 3-prime UTR variant associated with cardiovascular risk via altered ep... | Pharmacogenomics | Moderate | |
| 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 | |
| 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 | |
| rs17266594 | BANK1 Branch-point splice | Intronic branch-point variant in BANK1 that shifts isoform balance toward ful... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| 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 | |
| rs1801690 | APOH Trp316Ser | Missense variant in APOH (beta-2-glycoprotein I) that disrupts the phospholip... | Atherogenic Lipoproteins | Moderate | |
| rs11229030 | PRG2 | Intergenic tag SNP in the PRG2/PRG3 eosinophil major basic protein gene clust... | Allergy & Atopic Disease | Moderate | |
| rs12730735 | PTPN22 | Intronic PTPN22 haplotype tag variant that refines autoimmune risk stratifica... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs13196377 | TRAF3IP2 Intronic haplotype member | Intronic tagging variant in the TRAF3IP2/TRAF3IP2-AS1 locus that distinguishe... | Psoriasis & Spondyloarthropathy | Moderate | |
| 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 | |
| rs225011 | DIO2 | Intronic DIO2 variant nominally associated with Graves' disease susceptibilit... | Vitamin D Metabolism | Emerging | |
| 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 | |
| rs1310182 | PTPN22 PTPN22 Intron Variant (c.2054-852T>C) | Intronic PTPN22 variant in a transcription factor-binding site, associated wi... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs13210247 | TRAF3IP2 | Intronic variant in the TRAF3IP2 locus that lies within the antisense lncRNA ... | Psoriasis & Spondyloarthropathy | Strong | |
| 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 | |
| rs11465804 | IL23R | Intronic IL23R variant in strong linkage disequilibrium with the functional R... | IBD & Mucosal Immunity | Strong | |
| 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 | |
| rs201363394 | SERPING1 Arg400Cys | Pathogenic missense variant in SERPING1 encoding C1-inhibitor; the Arg400Cys ... | B-Cell Immunity & Antibody-Mediated Disease | Established | |
| rs12044149 | IL23R | Regulatory variant upstream of the IL-23 receptor gene more strongly associat... | IBD & Mucosal Immunity | Strong | |
| 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 | |
| rs187084 | TLR9 Promoter -1486T/C | Promoter variant that alters transcription factor binding and TLR9 expression... | Innate Immunity & Infection Defense | Moderate | |
| rs201408742 | GPR174 | X-linked intergenic variant near GPR174 (G protein-coupled receptor 174), a l... | TNF, NF-kB & Inflammatory Cytokines | Emerging | |
| rs2248932 | BLK Promoter/Intronic | Intronic BLK variant in the FAM167A-BLK regulatory locus that reduces B-lymph... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs116855232 | NUDT15 Arg139Cys | Nucleotide diphosphatase that inactivates toxic thiopurine metabolites; reduc... | Pharmacogenomics | Established | |
| 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 | |
| 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 | |
| rs11650354 | TBX21 TBX21 Region Variant | Intronic variant in TBX21 that forms a risk haplotype with rs16947078; the T ... | Allergy & Atopic Disease | 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 | |
| rs2736340 | BLK | FAM167A-BLK region regulatory variant that reduces B-lymphoid tyrosine kinase... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs1343151 | IL23R | Intronic IL23R variant whose minor A allele tags the protective haplotype for... | IBD & Mucosal Immunity | Moderate | |
| rs201227603 | HPS3 HPS3 Splice Donor Variant | Splice donor variant in HPS3 that disrupts exon 5 inclusion, causing Hermansk... | Innate Immunity & Infection Defense | Established | |
| 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 | |
| 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 | |
| rs4752 | GC GC rs4752 | Synonymous variant in vitamin D binding protein that tags distinct GC haploty... | Vitamin D Metabolism | Moderate | |
| 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 | |
| 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 | |
| rs2364480 | LTBR | Synonymous coding variant in the lymphotoxin-beta receptor gene associated wi... | Psoriasis & Spondyloarthropathy | Moderate | |
| 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 | |
| rs146582474 | SLC7A7 | Finnish founder splice acceptor mutation abolishing y+LAT1 transport activity... | Metabolic Enzymes & Rare Disorders | Established | |
| 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 | |
| rs3024505 | IL10 3' downstream variant | Downstream IL10 enhancer variant that disrupts a STAT3 binding site, reducing... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs3733197 | BANK1 A383T | BANK1 ankyrin-domain missense variant that amplifies B-cell receptor signalin... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs12133641 | IL6R IL-6 receptor intronic variant | Deep intronic IL6R variant associated with atopic dermatitis risk and systemi... | Allergy & Atopic Disease | Strong | |
| rs149007883 | NFKBIZ NFKBIZ p.Gly102Ala | Rare protective missense variant in the NF-kB inhibitor zeta gene that reduce... | Hormones & Sleep | 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 | |
| rs12044852 | CD58 | Intronic CD58 variant in strong LD with rs2300747 (r²=0.929); the C allele dr... | Neurology & Cognition | Strong | |
| 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 | |
| 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 | |
| rs403016 | FCGR3A | Rare missense variant in Fc gamma receptor IIIa (CD16a) causing an Arg36Ser s... | B-Cell Immunity & Antibody-Mediated Disease | Emerging | |
| rs419788 | SKIV2L | Intronic SKIV2L variant in the MHC class III region; the T allele tags an ind... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs17493811 | AGER | Tag SNP in the AGER 3′ downstream region associated with increased type 1 dia... | Hormones & Sleep | 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 | |
| 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 | |
| rs2476601 | PTPN22 R620W | The strongest non-HLA autoimmune risk allele, affecting T-cell and B-cell sig... | Autoimmune Tolerance & T-Cell Regulation | Established | |
| rs2501431 | CNR2 CNR2 rs2501431 | Synonymous coding variant in the cannabinoid receptor 2 gene that tags a hapl... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs3129878 | HLA-DRA HLA-DRA Variant | Intronic variant in the HLA class II region associated with nonobstructive az... | Endometriosis & Uterine Health | Strong | |
| 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 | |
| rs2488457 | PTPN22 | Promoter variant in PTPN22 that alters gene expression and modulates autoimmu... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs28940578 | MEFV M694I | Exon 10 missense variant in the inflammasome regulator pyrin, converting meth... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs35947132 | PRF1 A91V | Common perforin variant that reduces cytolytic activity by ~50%, acting as a ... | Innate Immunity & Infection Defense | Strong | |
| rs4840568 | BLK | Regulatory variant 2kb upstream of BLK that tags reduced B-lymphoid tyrosine ... | B-Cell Immunity & Antibody-Mediated Disease | 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 | |
| rs28940579 | MEFV V726A | Exon 10 missense variant in the inflammasome regulator pyrin; one of five fou... | TNF, NF-kB & Inflammatory Cytokines | 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 | |
| rs511278 | FCGR2A | Intronic FCGR2A variant in linkage disequilibrium with the H131R functional p... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| 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 | |
| rs1335532 | CD58 | Intronic CD58 variant that sits inside the miR-548ac stem-loop; the A allele ... | Neurology & Cognition | Strong | |
| rs28940580 | MEFV M680I | Exon 10 missense variant in the inflammasome regulator pyrin; one of five fou... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs3134883 | IL2RA | Intronic IL2RA variant independently associated with rheumatoid arthritis ris... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs3805435 | TNIP1 | Intronic variant in the GPX3/TNIP1 regulatory locus on chromosome 5; the C al... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs547154 | C2 IVS10 | Intronic C2 variant forming the H7 protective haplotype with CFB R32Q, reduci... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs1295685 | IL13 | 3'-UTR regulatory variant in IL13 that influences IL-13 mRNA stability and ex... | Allergy & Atopic Disease | 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 | |
| rs33996649 | PTPN22 R263Q | Protective loss-of-function variant in the PTPN22 catalytic domain that reduc... | Autoimmune Tolerance & T-Cell Regulation | 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 | |
| rs7514229 | TNFSF4 TNFSF4 OX40 ligand variant | Intronic variant in TNFSF4 that tags an upstream regulatory haplotype associa... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs1414273 | CD58 | Intronic CD58 variant hosting the miR-548ac stem-loop; the C allele creates a... | Neurology & Cognition | Strong | |
| rs2631367 | SLC22A5 OCTN2 -207C>G | Promoter variant in SLC22A5 (OCTN2) that reduces carnitine transporter expres... | IBD & Mucosal Immunity | Strong | |
| 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 | |
| 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 | |
| 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 | |
| rs3197999 | MST1 R689C | Macrophage-stimulating protein variant affecting innate immune response and I... | IBD & Mucosal Immunity | Strong | |
| rs3761847 | TRAF1 | Intronic GWAS variant in the TRAF1-C5 locus on chromosome 9 robustly associat... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs3789604 | RSBN1 | Synonymous RSBN1 variant that tags a PTPN22 locus haplotype independently ass... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs4406273 | HLA-C | Near-HLA-C intergenic variant that tags HLA-C*06:02 haplotype, conferring ris... | Psoriasis & Spondyloarthropathy | Strong | |
| rs498422 | LOC101929163 LOC101929163 Variant | Intronic variant in TSBP1-AS1 (LOC101929163), a non-coding antisense RNA in t... | Endometriosis & Uterine Health | Emerging | |
| 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 | |
| rs3816769 | STAT3 STAT3 co-variant | Intronic STAT3 variant where the T allele (reference, ~66%) increases risk fo... | TNF, NF-kB & Inflammatory Cytokines | Moderate | |
| rs41295061 | IL2RA | Regulatory variant in the IL2RA locus altering LEF1 transcription factor bind... | Autoimmune Tolerance & T-Cell Regulation | 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 | |
| rs2016105 | ELK3 ELK3 TSH regulatory variant | Intronic regulatory variant in ELK3 influencing circulating TSH levels and hy... | Hormones & Sleep | Strong | |
| rs3890745 | MMEL1 MMEL1 rs3890745 | Intronic variant near MMEL1 and TNFRSF14 on chromosome 1p36; the C allele is ... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs396991 | FCGR3A V158F | Missense variant in Fc gamma receptor IIIa (CD16a) that determines NK cell Ig... | Innate Immunity & Infection Defense | 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 | |
| rs72553883 | TNFRSF13B A181E | Transmembrane domain missense variant in TACI that abolishes NF-κB signaling,... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs9277535 | HLA-DPB1 | 3' UTR eQTL that reduces HLA-DPB1 expression, impairing antigen presentation ... | Interferon Signaling & Systemic Autoimmune | Strong | |
| rs1420101 | IL1RL1 | Intronic regulatory variant in IL1RL1 that lowers soluble ST2 (sST2) decoy re... | Allergy & Atopic Disease | Strong | |
| rs397515563 | DNAI1 DNAI1 IVS19+1G>A | Splice donor variant disrupting DNAI1 intron 19, causing in-frame deletion of... | Innate Immunity & Infection Defense | 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 | |
| rs7528684 | FCRL3 -169C>T | Promoter variant in FCRL3 that alters NF-κB binding and elevates FCRL3 expres... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs9378815 | IRF4 | Regulatory variant ~15 kb upstream of IRF4 that modulates germinal center B c... | Interferon Signaling & Systemic Autoimmune | 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 | |
| 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 | |
| rs17696736 | NAA25 NAA25 G/A | Intronic tag SNP at the 12q24 locus that captures SH2B3/LNK regulatory variat... | Blood Sugar & Diabetes | Strong | |
| rs492602 | FUT2 FUT2 secretor status proxy | A synonymous FUT2 proxy variant in strong LD with the W143X nonsense allele (... | IBD & Mucosal Immunity | Strong | |
| rs5029939 | TNFAIP3 | Intronic variant near TNFAIP3 that tags a 6q23 haplotype strongly associated ... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs7152376 | NFKBIA | Regulatory variant upstream of NFKBIA that specifically elevates risk of psor... | Psoriasis & Spondyloarthropathy | Moderate | |
| rs725613 | CLEC16A | Intronic variant in the autophagy regulator CLEC16A that alters thymic T-cell... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| 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 | |
| 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 | |
| rs516246 | FUT2 FUT2 rs516246 | Intronic FUT2 proxy variant tagging secretor status — whether ABO blood group... | IBD & Mucosal Immunity | Strong | |
| rs6920220 | TNFAIP3 | Regulatory variant upstream of TNFAIP3 that reduces A20 expression and impair... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs763361 | CD226 Gly307Ser | Missense variant in the T-cell and NK-cell co-stimulatory receptor CD226 (DNA... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs17250932 | TBX21 TBX21 Promoter Variant | Upstream promoter variant in TBX21 that reduces neonatal IL-5 and IL-13 secre... | Allergy & Atopic Disease | Emerging | |
| 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 | |
| rs4986790 | TLR4 Asp299Gly | Missense variant in Toll-like receptor 4 reducing bacterial endotoxin recogni... | Innate Immunity & Infection Defense | Strong | |
| rs689466 | PTGS2 A-1195G | Promoter variant in the PTGS2/COX-2 gene that reduces baseline COX-2 expressi... | IBD & Mucosal Immunity | 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 | |
| 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 | |
| rs6974491 | ELMO1 | Intronic ELMO1 variant acting as an eQTL that modulates engulfment and cell m... | IBD & Mucosal Immunity | Moderate | |
| rs7517847 | IL23R | Intronic IL23R variant in which the T allele increases susceptibility to Croh... | IBD & Mucosal Immunity | Strong | |
| rs7530511 | IL23R Leu310Pro | Missense variant in the IL-23 receptor that substitutes leucine for proline a... | IBD & Mucosal Immunity | Moderate | |
| rs5743836 | TLR9 Promoter -1237T/C | TLR9 promoter variant that creates an IL-6-responsive element and estrogen-se... | Innate Immunity & Infection Defense | Moderate | |
| rs187080438 | CTSS Cathepsin S antigen presentation variant | Intronic variant in the CTSS locus associated with elevated atopic dermatitis... | Allergy & Atopic Disease | Moderate | |
| rs7091565 | ANXA11 ANXA11 rs7091565 | 3' UTR variant in ANXA11 (annexin A11) in strong LD with the functional R230C... | Innate Immunity & Infection Defense | Moderate | |
| rs1885013 | RAD51B RAD51B Rheumatoid Arthritis Variant | Intronic variant in RAD51B (RAD51 paralog B), a DNA double-strand break repai... | Allergy & Atopic Disease | Moderate | |
| rs34536443 | TYK2 TYK2 p.Pro1104Ala | A missense variant in TYK2 that partially impairs JAK-family signaling downst... | Hormones & Sleep | Strong | |
| rs1898671 | TSLP TSLP Intronic Variant (Atopic Dermatitis) | Intronic TSLP variant that modulates thymic stromal lymphopoietin activity, w... | Allergy & Atopic Disease | Moderate | |
| 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 | |
| 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 | |
| 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 | |
| rs2243250 | IL4 IL4 -589C>T | Promoter polymorphism 589 bases upstream of the IL-4 transcription start site... | Allergy & Atopic Disease | 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 | |
| rs3194051 | IL7R I356V | Exon 8 missense variant in the IL-7 receptor alpha chain (Ile356Val) associat... | Neurology & Cognition | 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 | |
| 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 | |
| rs2872507 | IKZF3 | 17q21 regulatory variant in the IKZF3-ORMDL3-GSDMB locus with opposite effect... | Allergy & Atopic Disease | Strong | |
| 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 | |
| rs76428106 | FLT3 FLT3 Intronic Splice Variant | Low-frequency intronic variant in FLT3 that creates a cryptic splice site, tr... | Hormones & Sleep | 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 | |
| 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 | |
| rs689 | INS INS VNTR (Type 1 Diabetes Susceptibility) | Tag SNP for the insulin gene VNTR promoter — shorter Class I repeats raise T1... | Blood Sugar & Diabetes | Strong | |
| 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 | |
| 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 | |
| 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 | |
| rs6897932 | IL7R T244I | Splicing variant in the IL-7 receptor alpha chain that shifts the balance tow... | Neurology & Cognition | Strong | |
| 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 | |
| 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 | |
| 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 |