rs2228391

Parent Gene: TAP2

Importance: 5
Less common allele: C = 3%
More common allele: T = 97%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Graves Disease

The C allele of rs2228391 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 Thionamide-induced agranulocytosis in Graves' disease (trend).

Disease/Trait: Drug-Induced Agranulocytosis

The C allele of rs2228391 is reported to be associated with Drug-induced Agranulocytosis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Thionamide-induced agranulocytosis in Graves' disease (trend).

Disease/Trait: Response To Thioamide

The C allele of rs2228391 is reported to be associated with Response To Thioamide (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Thionamide-induced agranulocytosis in Graves' disease (trend).