The genes that we consider as definitely causal for CAD are MRAS (locus #13), EDNRA (also known as ETA, locus #14), JCAD (also known as KIAA1462, locus #29), SCARB1 (locus #39), FLT1 (also known as VEGFR1, locus #40), COL4A2/COL4A1 (locus #41), FURIN (locus #44), and PECAM1 (locus #48). This evidence concerns the gene FURIN and coronary artery disorder.