Tag
Immune System
109 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs10033900 | CFI | Intronic variant in complement factor I associated with age-related macular d... | Longevity & Aging | Strong | |
| rs1017861 | CHD7 CHD7 AIS susceptibility locus | Intronic variant in CHD7, a chromatin remodeler critical for neural crest cel... | Innate Immunity & Infection Defense | Moderate | |
| rs10206753 | IL1RL1 IL1RL1 TIR Domain Risk Haplotype | Missense variant in IL1RL1 encoding the Leu551Ser amino acid change in the in... | Allergy & Atopic Disease | 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 | |
| rs10208293 | IL1RL1 | Intronic IL1RL1 variant tagging an independent regulatory signal at the ST2 l... | Allergy & Atopic Disease | Moderate | |
| rs10832310 | CYP2R1 | Intronic tag SNP at the CYP2R1/PDE3B locus on chromosome 11 that marks a hapl... | Vitamin D Metabolism | Strong | |
| rs1016140 | CD58 | Intronic CD58 variant with a dual role — the G allele increases T-cell activi... | Neurology & Cognition | Moderate | |
| rs1048990 | PSMA6 PSMA6 -8C>G | 5'UTR variant that enhances PSMA6 transcription, amplifying proteasome-driven... | Innate Immunity & Infection Defense | Moderate | |
| rs1537415 | GLT6D1 | Intronic variant in GLT6D1 reducing GATA-3 transcription factor binding in T ... | Dental & Oral Health | Strong | |
| rs12785878 | DHCR7 Near gene T>G | Influences vitamin D synthesis by regulating how much 7-dehydrocholesterol is... | Vitamin D Metabolism | Strong | |
| rs1217414 | PTPN22 | Intronic PTPN22 variant independently associated with psoriasis and ankylosin... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs1270942 | CFB | Intronic variant in Complement Factor B associated with strongly elevated sys... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| 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 | |
| rs2235373 | IRF6 | Intronic IRF6 variant associated with non-syndromic cleft lip with or without... | Dental & Oral Health | 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 | |
| rs17266594 | BANK1 Branch-point splice | Intronic branch-point variant in BANK1 that shifts isoform balance toward ful... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs12730735 | PTPN22 | Intronic PTPN22 haplotype tag variant that refines autoimmune risk stratifica... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs150597413 | FLG S3247X | Nonsense variant eliminating filaggrin protein — a minor European FLG null al... | Skin & Eyes | Strong | |
| 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 | |
| rs2738058 | DEFA1A3 | Intergenic variant downstream of the DEFA1A3 alpha-defensin locus; T risk all... | Dental & Oral Health | 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 | |
| rs1800450 | MBL2 Gly54Asp (variant B) | Missense variant disrupting mannose-binding lectin oligomerization, reducing ... | Innate Immunity & Infection Defense | 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 | |
| rs2248932 | BLK Promoter/Intronic | Intronic BLK variant in the FAM167A-BLK regulatory locus that reduces B-lymph... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs3829251 | NADSYN1 | Intronic NADSYN1 variant at the DHCR7/NADSYN1 vitamin D locus; A allele was t... | Vitamin D Metabolism | Strong | |
| rs1978060 | TBX1 | Intronic variant in TBX1 acting as a cis-eQTL that reduces TBX1 expression an... | Innate Immunity & Infection Defense | Moderate | |
| rs2105325 | LOC100506023 LOC100506023 rs2105325 | Intronic variant in LOC100506023 (PRDX6-AS1) and TNFSF4 at the 1q25.1 locus, ... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs2736340 | BLK | FAM167A-BLK region regulatory variant that reduces B-lymphoid tyrosine kinase... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs11650680 | ORMDL3 ORMDL3 17q21 asthma susceptibility | Intronic regulatory variant in the ORMDL3 17q21 haploblock; the C allele driv... | Allergy & Atopic Disease | Strong | |
| rs230523 | NFKB1 | Intronic variant in the master immune transcription factor NF-κB1, associated... | Innate Immunity & Infection Defense | Strong | |
| rs34557412 | TNFRSF13B TACI C104R | Missense variant in the TACI receptor's cysteine-rich ligand-binding domain t... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs11808092 | EVI5 | Missense variant in EVI5's coiled-coil domain altering immune cell traffickin... | Neurology & Cognition | Strong | |
| rs3126085 | FLG | Intronic regulatory variant in the filaggrin gene locus that reduces FLG expr... | Skin & Eyes | Strong | |
| rs3733197 | BANK1 A383T | BANK1 ankyrin-domain missense variant that amplifies B-cell receptor signalin... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs26653 | ERAP1 | Missense variant (Arg127Pro) in ERAP1 that subtly alters ER peptide trimming ... | Psoriasis & Spondyloarthropathy | Strong | |
| rs705117 | GC | Intronic GC variant independently associated with vitamin D binding protein (... | Vitamin D Metabolism | Strong | |
| rs27044 | ERAP1 Gln730Glu | Missense variant in the ERAP1 C-terminal regulatory domain modulating peptide... | Psoriasis & Spondyloarthropathy | Moderate | |
| 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 | |
| rs403016 | FCGR3A | Rare missense variant in Fc gamma receptor IIIa (CD16a) causing an Arg36Ser s... | B-Cell Immunity & Antibody-Mediated Disease | Emerging | |
| rs7940244 | NADSYN1 Near DHCR7 | Intronic NADSYN1 variant in the DHCR7/NADSYN1 vitamin D locus; T allele tags ... | Vitamin D Metabolism | Strong | |
| rs12368672 | STAT6 STAT6 intronic variant | Deep intronic variant in STAT6 that modulates IL-4/IL-13 signal transduction;... | Allergy & Atopic Disease | 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 | |
| rs7944926 | DHCR7 | Near-gene intronic variant in the DHCR7/NADSYN1 locus on chromosome 11 that t... | Vitamin D Metabolism | Strong | |
| rs2476601 | PTPN22 R620W | The strongest non-HLA autoimmune risk allele, affecting T-cell and B-cell sig... | Autoimmune Tolerance & T-Cell Regulation | Established | |
| rs842999 | GC | Intronic GC variant tagging a haplotype associated with lower circulating 25-... | Vitamin D Metabolism | Moderate | |
| rs2488457 | PTPN22 | Promoter variant in PTPN22 that alters gene expression and modulates autoimmu... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| rs4840568 | BLK | Regulatory variant 2kb upstream of BLK that tags reduced B-lymphoid tyrosine ... | B-Cell Immunity & Antibody-Mediated Disease | Moderate | |
| rs558269137 | FLG 2282del4 | Frameshift deletion eliminating filaggrin protein, the second most common Eur... | Skin & Eyes | Established | |
| rs1831281 | CFH | Intronic CFH variant that tags the complement-risk haplotype; the C allele (c... | Vascular Inflammation & Remodeling | Moderate | |
| rs33980500 | TRAF3IP2 D10N | Missense variant in Act1 that abolishes IL-17 signaling by disrupting TRAF6 b... | Psoriasis & Spondyloarthropathy | Strong | |
| rs1335532 | CD58 | Intronic CD58 variant that sits inside the miR-548ac stem-loop; the A allele ... | Neurology & Cognition | Strong | |
| rs1831282 | CFH | Intronic CFH variant at chromosome 1q31.3 associated with AMD risk; the C all... | Vascular Inflammation & Remodeling | Strong | |
| rs3764880 | TLR8 A1G | X-linked initiator codon variant in TLR8 that fine-tunes the ratio of two TLR... | Innate Immunity & Infection Defense | Strong | |
| rs61816761 | FLG R501X | Nonsense variant eliminating filaggrin protein, the major genetic risk factor... | Skin & Eyes | Established | |
| rs33996649 | PTPN22 R263Q | Protective loss-of-function variant in the PTPN22 catalytic domain that reduc... | Autoimmune Tolerance & T-Cell Regulation | Strong | |
| rs3774937 | NFKB1 NFKB1 promoter/regulatory variant | Intronic NFKB1 variant with genome-wide significant associations with ulcerat... | Innate Immunity & Infection Defense | Strong | |
| rs1414273 | CD58 | Intronic CD58 variant hosting the miR-548ac stem-loop; the C allele creates a... | Neurology & Cognition | Strong | |
| 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 | |
| rs3789604 | RSBN1 | Synonymous RSBN1 variant that tags a PTPN22 locus haplotype independently ass... | Autoimmune Tolerance & T-Cell Regulation | Moderate | |
| 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 | |
| rs3804099 | TLR2 | Synonymous variant in Toll-Like Receptor 2 affecting mRNA stability and splic... | Innate Immunity & Infection Defense | Moderate | |
| rs13424006 | IL1RL1 | Intronic IL1RL1 variant in the 10th intron of the ST2 receptor gene; C allele... | Allergy & Atopic Disease | Moderate | |
| rs72553883 | TNFRSF13B A181E | Transmembrane domain missense variant in TACI that abolishes NF-κB signaling,... | B-Cell Immunity & Antibody-Mediated Disease | Strong | |
| rs4648127 | NFKB1 NFKB1 intronic variant | Rare protective intronic variant in the master immune transcription factor NF... | Innate Immunity & Infection Defense | Moderate | |
| rs4696480 | TLR2 T-16934A | Promoter variant in Toll-Like Receptor 2 that increases TLR2 expression, asso... | Innate Immunity & Infection Defense | Moderate | |
| rs4833095 | TLR1 N248S | Missense variant replacing asparagine with serine at TLR1 position 248 in the... | Innate Immunity & Infection Defense | Strong | |
| rs4986790 | TLR4 Asp299Gly | Missense variant in Toll-like receptor 4 reducing bacterial endotoxin recogni... | Innate Immunity & Infection Defense | Strong | |
| rs4986791 | TLR4 Thr399Ile | Missense variant in Toll-like receptor 4 that co-segregates with Asp299Gly on... | Innate Immunity & Infection Defense | Strong | |
| rs5743618 | TLR1 I602S | Coding variant replacing isoleucine with serine at TLR1 position 602, disrupt... | Innate Immunity & Infection Defense | Strong | |
| rs1800925 | IL13 -1112C>T | Promoter variant that selectively increases IL-13 expression in Th2 lymphocyt... | Allergy & Atopic Disease | Strong | |
| rs5743708 | TLR2 R753Q | Missense variant in Toll-Like Receptor 2 impairing innate immune signaling to... | Innate Immunity & Infection Defense | Strong | |
| rs8018720 | SEC23A | Missense variant in the COPII vesicle coat protein SEC23A, associated with ci... | Metabolic Enzymes & Rare Disorders | Emerging | |
| rs1801275 | IL4R Q576R | Gain-of-function missense variant in the IL-4 receptor alpha chain that ampli... | Allergy & Atopic Disease | 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 | |
| rs1805011 | IL4R IL4R Glu375Ala | Missense variant in the extracellular domain of the IL-4 receptor alpha chain... | Allergy & Atopic Disease | Moderate | |
| rs6519605 | TBX1 | Intergenic variant on chromosome 22q11 (merged into rs133255) located downstr... | Innate Immunity & Infection Defense | Emerging | |
| rs1837253 | TSLP Upstream Variant | Upstream regulatory variant in TSLP reducing cytokine expression; the protect... | Allergy & Atopic Disease | Strong | |
| rs187080438 | CTSS Cathepsin S antigen presentation variant | Intronic variant in the CTSS locus associated with elevated atopic dermatitis... | Allergy & Atopic Disease | Moderate | |
| rs1885013 | RAD51B RAD51B Rheumatoid Arthritis Variant | Intronic variant in RAD51B (RAD51 paralog B), a DNA double-strand break repai... | Allergy & Atopic Disease | Moderate | |
| rs551397 | CFH | Intronic CFH variant that tags the AMD-risk haplotype; the C allele tracks co... | Longevity & Aging | Moderate | |
| 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 | |
| rs2070874 | IL4 IL4 C-33T | 5'-UTR variant 33 bases downstream of the IL-4 transcription start site; the ... | 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 | |
| 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 | |
| rs2872507 | IKZF3 | 17q21 regulatory variant in the IKZF3-ORMDL3-GSDMB locus with opposite effect... | Allergy & Atopic Disease | Strong | |
| rs76428106 | FLT3 FLT3 Intronic Splice Variant | Low-frequency intronic variant in FLT3 that creates a cryptic splice site, tr... | Hormones & Sleep | Strong | |
| rs3771166 | IL1RL1/IL18R1 | GABRIEL Consortium lead GWAS SNP at the IL1RL1/IL18R1 locus on chromosome 2q1... | Allergy & Atopic Disease | Strong | |
| rs3806933 | TSLP | Functional promoter variant in TSLP that creates an AP-1 transcription factor... | Allergy & Atopic Disease | Moderate | |
| 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 | |
| rs7216389 | GSDMB ORMDL3 17q21 asthma risk | Intronic GSDMB variant that acts as an eQTL for ORMDL3; the T allele elevates... | Allergy & Atopic Disease | Established | |
| 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 | |
| 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 |