Genetic variations that influence DNA repair efficiency may contribute to coronary artery disease (CAD) susceptibility. Previous studies have investigated whether there was evidence of an association
Genome-wide association studies identified a strong signal for non coding variants at the 1p21.2 locus associated with calcific aortic valve stenosis (CAVS). Regulation at the locus and impact on the
Supplementary Material 1: Table S1: List of 19 diseases including cardiovascular diseasesand their comorbidities and their definitions. Table S2: Percentage of sample overlap between FinnGen genome-wi
Secondary structure in the H19 transcript, which is altered through a SNP in DCM patients, is an attractive target for future studies investigating the molecular mechanism by which H19 contributes to