{{Rsnum
|rsid=121918530
|Gene=MEF2A
|Chromosome=15
|position=99690352
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MEF2A
}}{{omim
|id=600660
|rsnum=121918530
|variant=0003
}}{{ClinVar
|rsid=121918530
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=100230557
|CHROM=15
|GMAF=0.0009
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=MEF2A:4205
|GENE_NAME=MEF2A
|GENE_ID=4205
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.100230557A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNACC=RCV000009506.3
|CLNDBN=Coronary artery disease/myocardial infarction
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600660.0003
|COMMON=1
|Disease=Coronary artery disease/myocardial infarction
}}