{{Rsnum
|rsid=121913630
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH7
|position=23425814
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160760
|rsnum=121913630
|variant=0008
}}{{ClinVar
|rsid=121913630
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=23895023
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYH7:4625
|GENE_NAME=MYH7
|GENE_ID=4625
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000014.8:g.23895023G>A; NC_000014.8:g.23895023G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160760.0008
|CLNSIG=5
|CLNCUI=CN030093
|CLNDBN=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|Disease=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000015151.24; RCV000035772.1; RCV000035771.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1385:NBK1768:CN030093:192600; NBK1768:C0949658:83978005
}}