Tag
Skin Health
57 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs121434287 | SLC39A4 SLC39A4 zinc transporter variant | Pathogenic missense variant in the intestinal zinc transporter ZIP4, causing ... | Iron & Mineral Transport | Established | |
| rs10794648 | IFNLR1/GRHL3 | Intergenic regulatory variant near IFNLR1 that contacts GRHL3 via chromatin l... | Interferon Signaling & Systemic Autoimmune | Moderate | |
| rs121434289 | SLC39A4 Gly374Arg | Missense variant in ZIP4 zinc transporter causing total loss of intestinal zi... | Iron & Mineral Transport | Established | |
| 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 | |
| rs11079788 | TBX21 TBX21 Regulatory Variant | Intronic regulatory variant in TBX21 that influences T-bet expression and Th1... | Allergy & Atopic Disease | Emerging | |
| rs121434292 | SLC39A4 Arg95Cys | Pathogenic missense variant in ZIP4, the primary intestinal zinc transporter,... | Iron & Mineral Transport | Established | |
| rs11204971 | FLG FLG locus regulatory variant | Regulatory tag SNP in the filaggrin (FLG) locus associated with reduced FLG e... | Allergy & Atopic Disease | Moderate | |
| rs17881320 | STAT3 JAK-STAT3 Signaling Variant | Intronic STAT3 variant associated with increased atopic dermatitis risk (OR=1... | TNF, NF-kB & Inflammatory Cytokines | Strong | |
| rs150597413 | FLG S3247X | Nonsense variant eliminating filaggrin protein — a minor European FLG null al... | Skin & Eyes | 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 | |
| rs115161931 | CTSS | Independent CTSS-locus GWAS signal for atopic dermatitis on chromosome 1q21.3... | Allergy & Atopic Disease | Moderate | |
| rs200482978 | SLC39A4 | Pathogenic nonsense variant in the intestinal zinc transporter ZIP4, creating... | Iron & Mineral Transport | Established | |
| rs17728338 | TNIP1 TNIP1/ABIN1 variant | Intergenic regulatory variant near TNIP1 whose A allele reduces ABIN1-mediate... | Psoriasis & Spondyloarthropathy | Strong | |
| rs1805007 | MC1R R151C | Strongest "R" allele in the melanocortin-1 receptor, shifting pigment from ph... | Skin & Eyes | Established | |
| rs182506368 | SLC39A4 SLC39A4 p.Ala99Thr | Pathogenic missense variant in the ZIP4 intestinal zinc transporter causing h... | Vitamins & Nutrient Absorption | Established | |
| rs12123821 | FLG Filaggrin skin barrier variant | Common regulatory variant in the FLG locus associated with impaired skin barr... | Allergy & Atopic Disease | Strong | |
| rs3126085 | FLG | Intronic regulatory variant in the filaggrin gene locus that reduces FLG expr... | Skin & Eyes | Strong | |
| rs12133641 | IL6R IL-6 receptor intronic variant | Deep intronic IL6R variant associated with atopic dermatitis risk and systemi... | Allergy & Atopic Disease | Strong | |
| rs12251307 | IL2RA IL-2 receptor alpha chain variant | Intergenic variant 19 kb downstream of IL2RA associated with atopic dermatiti... | Allergy & Atopic Disease | Strong | |
| rs397507563 | FLG 3702delG | Frameshift deletion in the third filaggrin repeat domain — the third most com... | Skin & Eyes | Established | |
| rs558269137 | FLG 2282del4 | Frameshift deletion eliminating filaggrin protein, the second most common Eur... | Skin & Eyes | Established | |
| rs33980500 | TRAF3IP2 D10N | Missense variant in Act1 that abolishes IL-17 signaling by disrupting TRAF6 b... | Psoriasis & Spondyloarthropathy | 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 | |
| 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 | |
| rs4406273 | HLA-C | Near-HLA-C intergenic variant that tags HLA-C*06:02 haplotype, conferring ris... | Psoriasis & Spondyloarthropathy | Strong | |
| 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 | |
| rs167769 | STAT6 | Intronic variant in STAT6 (intron 2) that forms a functional haplotype with r... | Allergy & Atopic Disease | Strong | |
| rs4696480 | TLR2 T-16934A | Promoter variant in Toll-Like Receptor 2 that increases TLR2 expression, asso... | Innate Immunity & Infection Defense | Moderate | |
| rs17250932 | TBX21 TBX21 Promoter Variant | Upstream promoter variant in TBX21 that reduces neonatal IL-5 and IL-13 secre... | Allergy & Atopic Disease | Emerging | |
| 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 | |
| rs1801275 | IL4R Q576R | Gain-of-function missense variant in the IL-4 receptor alpha chain that ampli... | Allergy & Atopic Disease | Strong | |
| rs1805011 | IL4R IL4R Glu375Ala | Missense variant in the extracellular domain of the IL-4 receptor alpha chain... | Allergy & Atopic Disease | Moderate | |
| rs187080438 | CTSS Cathepsin S antigen presentation variant | Intronic variant in the CTSS locus associated with elevated atopic dermatitis... | Allergy & Atopic Disease | Moderate | |
| rs1898671 | TSLP TSLP Intronic Variant (Atopic Dermatitis) | Intronic TSLP variant that modulates thymic stromal lymphopoietin activity, w... | Allergy & Atopic Disease | Moderate | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| rs3024971 | STAT6 | Intronic variant in STAT6 near the 3' end of the gene that modulates STAT6 mR... | Allergy & Atopic Disease | Moderate | |
| 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 | |
| rs3806933 | TSLP | Functional promoter variant in TSLP that creates an AP-1 transcription factor... | Allergy & Atopic Disease | Moderate | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| rs992969 | IL33 | Regulatory variant upstream of IL33 encoding interleukin-33; the A allele inc... | Allergy & Atopic Disease | Strong |