{{Rsnum
|rsid=121913644
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH7
|position=23425798
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160760
|rsnum=121913644
|variant=0025
}}{{ClinVar
|rsid=121913644
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=23895007
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=MYH7:4625
|GENE_NAME=MYH7
|GENE_ID=4625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.23895007G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160760.0025
|CLNSIG=5
|CLNCUI=CN030093
|CLNDBN=Familial hypertrophic cardiomyopathy 1; AllHighlyPenetrant
|Disease=Familial hypertrophic cardiomyopathy 1; AllHighlyPenetrant
|CLNACC=RCV000015167.24; RCV000035776.1
|Tags=RV;PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=NBK1385:NBK1768:CN030093:192600; CN169374
}}