rs2233278

This is a regulatory region variant variant in the TNIP1 gene.

GWAS Catalog Trait Associations (4)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

psoriasis

Allele C
OR 1.59
p 2.0e-42
N 33,394
Large GWAS
European
Allele C
OR 0.37
p 2.0e-20
N 394,626
Large GWAS
European
Allele C
OR 1.65
p 1.0e-18
N 12,244
Large GWAS
European

psoriasis vulgaris

Allele C
OR 1.66
p 4.0e-37
N 8,941
Large GWAS
European
Hirata J et al. Variants at HLA-A, HLA-C, and HLA-DQB1 Confer Risk of Psoriasis Vulgaris in Japanese. The Journal of Investigative Dermatology 138(3):542-548 (2018)
Allele C
OR 1.96
p 4.0e-10
N 708
Small GWAS
East Asian

psoriasis, type 2 diabetes mellitus

Patrick MT et al. Causal Relationship and Shared Genetic Loci between Psoriasis and Type 2 Diabetes through Trans-Disease Meta-Analysis. The Journal of Investigative Dermatology 141(6):1493-1502 (2021)
Allele C
OR 1.26
p 5.0e-30
N 925,490
Meta-analysisLarge GWAS
European

About TNIP1

This gene encodes an A20-binding protein which plays a role in autoimmunity and tissue homeostasis through the regulation of nuclear factor kappa-B activation. Mutations in this gene have been associated with psoriatic arthritis, rheumatoid arthritis, and systemic lupus erythematosus. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]

View all TNIP1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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