Research
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