MEF2A and coronary artery disorder: In some studies, the MEF2 gene variants c.704C>A (p.S235Y), c.812C>G (p.P271R), c.836C>T (p.P279L), c.848G>A (p.G283D) missenses, c.1315C>T (p.R439X) nonsense, and seven out-of-frame deletions were predicted as disease-causing variants for CAD [59].