rs12101261

Parent Gene: BHLHB9P1, TSHR

Importance: 2
Less common allele: T = 42%
More common allele: C = 58%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Graves Disease

The T allele of rs12101261 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.