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rs10206753
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IL1RL1
IL1RL1 TIR Domain Risk Haplotype
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Missense variant in IL1RL1 encoding the Leu551Ser amino acid change in the in...
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Allergy & Atopic Disease
|
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Strong
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|
rs11652075
|
CARD14
CARD14 Arg820Trp (R820W)
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Missense variant in the keratinocyte NF-κB scaffold protein CARD14 that modes...
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Psoriasis & Spondyloarthropathy
|
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Strong
|
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rs12188300
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IL12B
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Near-gene variant at the IL12B locus associated with psoriasis risk through a...
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Psoriasis & Spondyloarthropathy
|
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Moderate
|
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rs12191877
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HLA-C
Tag for *06:02
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Tag SNP for HLA-C*06:02, the strongest genetic risk factor for psoriasis, det...
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Psoriasis & Spondyloarthropathy
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Established
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rs12883343
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NFKBIA
NFKBIA/IkB-alpha variant
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Regulatory variant near NFKBIA that specifically elevates risk for psoriatic ...
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Psoriasis & Spondyloarthropathy
|
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Moderate
|
|
rs13190932
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TRAF3IP2
R74W
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Missense variant in the IL-17 adaptor Act1 (Arg74Trp) that is the primary GWA...
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Psoriasis & Spondyloarthropathy
|
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Strong
|
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rs17881320
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STAT3
JAK-STAT3 Signaling Variant
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Intronic STAT3 variant associated with increased atopic dermatitis risk (OR=1...
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TNF, NF-kB & Inflammatory Cytokines
|
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Strong
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|
rs13196377
|
TRAF3IP2
Intronic haplotype member
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Intronic tagging variant in the TRAF3IP2/TRAF3IP2-AS1 locus that distinguishe...
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Psoriasis & Spondyloarthropathy
|
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Moderate
|
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rs11465770
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IL23R
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Intronic IL23R variant whose minor T allele tags a protective haplotype that ...
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IBD & Mucosal Immunity
|
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Moderate
|
|
rs13210247
|
TRAF3IP2
|
Intronic variant in the TRAF3IP2 locus that lies within the antisense lncRNA ...
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Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs16840252
|
CTLA4
|
Upstream promoter variant (~1147 bp 5' of CTLA4) tagging an autoimmune-associ...
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Autoimmune Tolerance & T-Cell Regulation
|
|
Moderate
|
|
rs2066808
|
IL23A
|
Intronic variant near IL23A encoding the IL-23 p19 subunit; G allele increase...
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Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs2233434
|
NFKBIE
|
Missense variant in NFKBIE (IκBε) reducing the inhibitory capacity of the IκB...
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TNF, NF-kB & Inflammatory Cytokines
|
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Strong
|
|
rs2546890
|
LOC285626
LOC285626 rs2546890
|
Regulatory variant upstream of IL12B associated with increased risk of multip...
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Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs12133641
|
IL6R
IL-6 receptor intronic variant
|
Deep intronic IL6R variant associated with atopic dermatitis risk and systemi...
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Allergy & Atopic Disease
|
|
Strong
|
|
rs3212227
|
IL12B
3'UTR
|
IL12B 3'-UTR variant forming the canonical two-SNP psoriasis risk haplotype w...
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Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs4810485
|
CD40
|
Intronic variant in CD40 regulating B-cell surface expression; the G allele d...
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B-Cell Immunity & Antibody-Mediated Disease
|
|
Strong
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|
rs660895
|
HLA-DRB1
|
Regulatory tag SNP in the HLA-DRB1 region; the G allele marks the HLA-DRB1*04...
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Interferon Signaling & Systemic Autoimmune
|
|
Strong
|
|
rs3213094
|
IL12B
Promoter-region
|
Intronic IL12B variant in linkage with the promoter-regulatory haplotype; T a...
|
Psoriasis & Spondyloarthropathy
|
|
Moderate
|
|
rs33980500
|
TRAF3IP2
D10N
|
Missense variant in Act1 that abolishes IL-17 signaling by disrupting TRAF6 b...
|
Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs1342326
|
IL33
IL33 regulatory variant
|
Regulatory variant upstream of IL33; the C allele elevates IL-33 expression, ...
|
Allergy & Atopic Disease
|
|
Strong
|
|
rs1420101
|
IL1RL1
|
Intronic regulatory variant in IL1RL1 that lowers soluble ST2 (sST2) decoy re...
|
Allergy & Atopic Disease
|
|
Strong
|
|
rs4845625
|
IL6R
|
Intronic IL6R variant associated with coronary artery disease risk, elevated ...
|
TNF, NF-kB & Inflammatory Cytokines
|
|
Moderate
|
|
rs61751629
|
CARD14
Glu422Lys
|
Rare missense variant in the keratinocyte NF-κB scaffold protein CARD14 that ...
|
Psoriasis & Spondyloarthropathy
|
|
Emerging
|
|
rs4537545
|
IL6R
IL6R intron variant
|
Intronic IL6R variant in linkage disequilibrium with the functional Asp358Ala...
|
Coronary Artery Disease & Atherosclerosis
|
|
Strong
|
|
rs6887695
|
IL12B
Upstream regulatory
|
Upstream regulatory variant ~60 kb 5' of IL12B, forming the canonical two-SNP...
|
Psoriasis & Spondyloarthropathy
|
|
Strong
|
|
rs7152376
|
NFKBIA
|
Regulatory variant upstream of NFKBIA that specifically elevates risk of psor...
|
Psoriasis & Spondyloarthropathy
|
|
Moderate
|
|
rs7746808
|
IL23A
|
Intergenic variant near the IL23A locus associated with psoriasis and psoriat...
|
Psoriasis & Spondyloarthropathy
|
|
Emerging
|
|
rs1805010
|
IL4R
Ile75Val
|
Missense variant in the extracellular domain of the IL-4 receptor alpha chain...
|
Allergy & Atopic Disease
|
|
Moderate
|
|
rs20541
|
IL13
R130Q
|
Missense variant in IL-13 that enhances Th2 cytokine signaling, elevating ser...
|
Allergy & Atopic Disease
|
|
Strong
|
|
rs2228145
|
IL6R
Asp358Ala
|
Missense variant in the IL-6 receptor that increases receptor shedding and en...
|
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
|
|
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
|