Fig. 2From: A genetic variant c.553G > T (rs2075291) in the apolipoprotein A5 gene is associated with altered triglycerides levels in coronary artery disease (CAD) patients with lipid lowering drugLipid profiles levels in homozygous and heterozygous T allele patients with CAD separated by APOA5 genotype. The variants (GT and TT) are defined by the presence of c.553G > TSNPBack to article page