{{Rsnum
|rsid=397514655
|Chromosome=5
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=MEF2C
|position=88804743
|Gene_s=MEF2C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=5
|CLNACC=RCV000033229.2
|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.88100560A>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600662.0002
|Disease=Mental retardation
|FwdALT=A
|FwdREF=T
|GENEINFO=MEF2C:4208
|GENE_ID=4208
|GENE_NAME=MEF2C
|REF=A
|RSPOS=88100560
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514655
}}