[PMID 19956433] Genetics of coronary artery disease: focus on genome-wide association studies.


rs3127599

Parent Gene: LPA, LPAL2, SLC22A3

Importance: 5
Less common allele: T = 23%
More common allele: C = 77%
My Genotype: Log In
Risk Allele: T, C

Disease/Trait: Coronary Heart Disease

The T allele of rs3127599 is reported to be associated with Coronary Heart Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Coronary heart disease.

Disease/Trait: Coronary Heart Disease

The C allele of rs3127599 is reported to be associated with Coronary Heart Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Coronary heart disease.