{{Rsnum
|rsid=367543053
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYH7
|position=23412855
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=14
|CLNACC=RCV000034923.1
|CLNALLE=1
|CLNDBN=Congenital myopathy with fiber type disproportion
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1259:C0546264:255310:2020:240084007
|CLNHGVS=NC_000014.8:g.23882064T>C
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1259
|Disease=Congenital myopathy with fiber type disproportion
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=23882064
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=367543053
|GENEINFO=MYH7:4625
|GENE_ID=4625
|GENE_NAME=MYH7
}}{{PMID Auto
|PMID=21288719
|Title=A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy.
}}