PEMT rs12936587 variant was associated with increased susceptibility to CAD (OR 1.07, 95% CI 1.05–1.09, p = 4.45x10−10) (Schunkert et al., 2011) in a meta-analysis of 14 GWAS (22,233 cases of CAD and 64,762 controls). The gene discussed is PEMT; the disease is coronary artery disorder.