rs61361928

Parent Gene: UGT2B7

Importance: 5
Less common allele: C = 0%
More common allele: T = 100%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Acute Coronary Syndrome

The T allele of rs61361928 is reported to be associated with Acute Coronary Syndrome (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor.

Disease/Trait: Ar-C124910xx Measurement

The T allele of rs61361928 is reported to be associated with Ar-c124910xx Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor.