
The study investigates the link between genetic variants in lipid metabolism-related genes and coronary artery disease (CAD) in a Chinese Han population. Using next-generation sequencing, rare and common variants in 12 genes were analyzed in 252 individuals (120 CAD patients, 132 healthy controls). A common variant, LIPC rs6083, showed a significant association with CAD. Thirty-three rare variants were identified, though no significant gene-based association was found. This suggests targeted sequencing can reveal both common and rare variants, with LIPC rs6083 possibly offering protection against CAD.
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