{{Rsnum
|rsid=121918529
|Gene=MEF2A
|Chromosome=15
|position=99690400
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MEF2A
}}{{omim
|id=600660
|rsnum=121918529
|variant=0002
}}{{ClinVar
|rsid=121918529
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=100230605
|CHROM=15
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=MEF2A:4205
|GENE_NAME=MEF2A
|GENE_ID=4205
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.100230605C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000009505.1
|CLNDBN=Coronary artery disease/myocardial infarction
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600660.0002
|COMMON=0
|Disease=Coronary artery disease/myocardial infarction
}}