rs3893464

Parent Gene: HCG9, HLA-A

Importance: 4
Less common allele: G = 49%
More common allele: A = 51%
My Genotype: Log In
Risk Allele: G

Disease/Trait: Graves Disease

The G allele of rs3893464 is reported to be associated with Graves Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Graves' disease.