{{Rsnum
|rsid=367543052
|Chromosome=14
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AGA)
|geno3=(AGA;AGA)
|Gene=MYH7
|position=23415476
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=14
|CLNACC=RCV000034922.1; RCV000035952.1
|CLNALLE=1
|CLNDBN=Congenital myopathy with fiber type disproportion; Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1259:C0546264:255310:2020:240084007; NBK1768:C0949658:83978005
|CLNHGVS=NC_000014.8:g.23884685_23884687delTCT
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1259
|Disease=Congenital myopathy with fiber type disproportion; Primary familial hypertrophic cardiomyopathy
|FwdREF=AGA
|REF=ATCT
|RSPOS=23884684
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=367543052
|GENEINFO=MYH7:4625
|GENE_ID=4625
|GENE_NAME=MYH7
}}{{PMID Auto
|PMID=20733148
|Title=MYH7 gene tail mutation causing myopathic profiles beyond Laing distal myopathy.
}}