rs10200159
This is a coding sequence variant variant in the PPP4R3B gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Vitiligo
Jin Y et al. “Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants.” Nature Genetics 48(11):1418-1424 (2016)
Allele C
OR 1.51
p 4.0e-19
N 40,258
Large GWAS
European
About PPP4R3B
Predicted to enable protein phosphatase activator activity. Involved in regulation of double-strand break repair. Located in centrosome; chromatin; and nuclear speck. Part of protein phosphatase 4 complex. [provided by Alliance of Genome Resources, Jul 2025]
View all PPP4R3B variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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