The one variant (rs118042209) in the credible set of TMEM200A locus was associated with multiple disease endpoints representing major coronary heart disease (CHD) in FinnGen, including coronary atherosclerosis, ischemic heart disease and angina pectoris, whereas the lead variant in the PRG3 locus was associated with cardiomyopathy. This evidence concerns the gene PRG3 and coronary artery disorder.