|
rs10794648
|
IFNLR1/GRHL3
|
Intergenic regulatory variant near IFNLR1 that contacts GRHL3 via chromatin l...
|
Interferon Signaling & Systemic Autoimmune
|
|
Moderate
|
|
rs11652075
|
CARD14
CARD14 Arg820Trp (R820W)
|
Missense variant in the keratinocyte NF-κB scaffold protein CARD14 that modes...
|
Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs12188300
|
IL12B
|
Near-gene variant at the IL12B locus associated with psoriasis risk through a...
|
Psoriasis & Spondyloarthropathy
|
|
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
|
|
rs115161931
|
CTSS
|
Independent CTSS-locus GWAS signal for atopic dermatitis on chromosome 1q21.3...
|
Allergy & Atopic Disease
|
|
Moderate
|
|
rs17728338
|
TNIP1
TNIP1/ABIN1 variant
|
Intergenic regulatory variant near TNIP1 whose A allele reduces ABIN1-mediate...
|
Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs2066808
|
IL23A
|
Intronic variant near IL23A encoding the IL-23 p19 subunit; G allele increase...
|
Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs2256774
|
IL2RA
|
Intronic IL2RA variant that modulates soluble IL-2RA shedding and Treg signal...
|
Autoimmune Tolerance & T-Cell Regulation
|
|
Moderate
|
|
rs12123821
|
FLG
Filaggrin skin barrier variant
|
Common regulatory variant in the FLG locus associated with impaired skin barr...
|
Allergy & Atopic Disease
|
|
Strong
|
|
rs3212227
|
IL12B
3'UTR
|
IL12B 3'-UTR variant forming the canonical two-SNP psoriasis risk haplotype w...
|
Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs3213094
|
IL12B
Promoter-region
|
Intronic IL12B variant in linkage with the promoter-regulatory haplotype; T a...
|
Psoriasis & Spondyloarthropathy
|
|
Moderate
|
|
rs3805435
|
TNIP1
|
Intronic variant in the GPX3/TNIP1 regulatory locus on chromosome 5; the C al...
|
Psoriasis & Spondyloarthropathy
|
|
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
|
|
rs61751629
|
CARD14
Glu422Lys
|
Rare missense variant in the keratinocyte NF-κB scaffold protein CARD14 that ...
|
Psoriasis & Spondyloarthropathy
|
|
Emerging
|
|
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
|
|
rs6887695
|
IL12B
Upstream regulatory
|
Upstream regulatory variant ~60 kb 5' of IL12B, forming the canonical two-SNP...
|
Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs7746808
|
IL23A
|
Intergenic variant near the IL23A locus associated with psoriasis and psoriat...
|
Psoriasis & Spondyloarthropathy
|
|
Emerging
|
|
rs187080438
|
CTSS
Cathepsin S antigen presentation variant
|
Intronic variant in the CTSS locus associated with elevated atopic dermatitis...
|
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
|
|
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
|
|
rs7927894
|
EMSY
|
Regulatory variant near the EMSY/C11orf30 locus; T allele increases EMSY expr...
|
Allergy & Atopic Disease
|
|
Strong
|