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
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
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
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
