rs7753873
This is a regulatory region variant variant in the WAKMAR2 gene.
▶Research that mentions this SNP (1)
▶TNFAIP3 gene polymorphisms confer risk for Behcet’s disease in a Chinese Han populationAssociationN=2,137Hong Li et al.(2013)· Human Genetics
TNFAIP3 gene polymorphisms confer risk for Behcet’s disease in a Chinese Han population
AssociationN=2,137Hong Li et al.(2013)· Human Genetics
This candidate gene association study examined five TNFAIP3 SNPs (rs10499194, rs610604, rs7753873, rs5029928, rs9494885) in 722 Chinese Han Behcet's disease patients and 1,415 controls. The strongest association was rs9494885 with BD (TC genotype OR=2.03, p=1.83×10⁻¹⁰), while rs10499194 and rs7753873 showed weaker associations. The rs9494885 TT genotype was protective (OR=0.50, p=1.23×10⁻¹⁰).
Traits studied:Behcet's disease
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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