rs2048327 is a SNP in the SLC22A3 gene. The recessive model is associated with a reduced coronary artery disease (CAD) risk.

The C/C genotype was associated with a reduced risk of coronary artery disease (CAD) (OR=0.60; p = 0.036) [R].

rs2048327

Parent Gene: LPA, LPAL2, SLC22A3

Importance: 4
Less common allele: C = 29%
More common allele: T = 71%
My Genotype: Log In
Risk Allele: C, C, C

Disease/Trait: Coronary Heart Disease

The C allele of rs2048327 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 rs2048327 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 rs2048327 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 artery disease.