rs3823355

Parent Gene: HCG9, HLA-A

Importance: 3
Less common allele: T = 26%
More common allele: C = 74%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Vitiligo

The T allele of rs3823355 is reported to be associated with Vitiligo (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Vitiligo.