Parent Gene: C10ORF32-ASMT, CYP17A1

Importance: 4
Less common allele: G = 18%
More common allele: T = 82%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Coronary Artery Disease

The T allele of rs11191416 is reported to be associated with Coronary Artery Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Coronary artery disease.