{{Rsnum
|rsid=121918531
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MEF2A
|position=99690412
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MEF2A
}}{{omim
|id=600660
|rsnum=121918531
|variant=0004
}}{{ClinVar
|rsid=121918531
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=100230617
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MEF2A:4205
|GENE_NAME=MEF2A
|GENE_ID=4205
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.100230617G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000009507.1
|CLNDBN=Coronary artery disease/myocardial infarction
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600660.0004
|Disease=Coronary artery disease/myocardial infarction
}}