{{Rsnum
|rsid=371898076
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH7
|position=23426833
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000035758.1
|CLNALLE=1
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|CLNHGVS=NC_000014.8:g.23896042C>T
|CLNSIG=5
|Disease=Primary familial hypertrophic cardiomyopathy
|FwdALT=T
|FwdREF=C
|GENEINFO=MYH7:4625
|GENE_ID=4625
|GENE_NAME=MYH7
|REF=C
|RSPOS=23896042
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=SNV
|VP=0x050260000000000002100100
|WGT=0
|dbSNPBuildID=138
|rsid=371898076
}}