{{Rsnum
|rsid=121913654
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH7
|position=23415176
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160760
|rsnum=121913654
|variant=0037
}}{{ClinVar
|rsid=121913654
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=23884385
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MYH7:4625
|GENE_NAME=MYH7
|GENE_ID=4625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.23884385A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160760.0037
|CLNSIG=5
|CLNCUI=C1842160; CN030093
|CLNDBN=Myopathy, myosin storage; Familial hypertrophic cardiomyopathy 1; Left ventricular noncompaction 5
|Disease=Myopathy; Familial hypertrophic cardiomyopathy 1; Left ventricular noncompaction 5
|CLNACC=RCV000015181.24; RCV000015182.24; RCV000015183.24
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM; GeneReviews:GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=C1842160:608358; NBK1385:NBK1768:CN030093:192600; C3150690
}}