MEF2A and coronary artery disorder: Similar cohort studies in Chinese Han subjects claim that the 3′ UTR may consist of functionally relevant nucleotide changes, and 2 single nucleotide polymorphisms were detected but deemed not significant, but a further haplotype carrier of rs325380-rs325381 was claimed to be associated with CAD risk, suggesting variance in the 3′ UTR of MEF-2A [175].