{{Rsnum
|rsid=267607233
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MEF2C
|position=88731856
|Gene_s=MEF2C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=5
|CLNACC=RCV000009503.1
|CLNALLE=1
|CLNDBN=Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3150700:613443:228384
|CLNHGVS=NC_000005.9:g.88027673G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600662.0001
|Disease=Mental retardation
|FwdALT=G
|FwdREF=C
|GENEINFO=MEF2C:4208
|GENE_ID=4208
|GENE_NAME=MEF2C
|REF=G
|RSPOS=88027673
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607233
}}