{{Rsnum
|rsid=397516275
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=MYH7
|position=23430591
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CHROM=14
|CLNACC=RCV000036013.1; RCV000036012.1
|CLNALLE=1; 2
|CLNDBN=AllHighlyPenetrant; Primary familial hypertrophic cardiomyopathy
|CLNDSDB=MedGen; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=CN169374; NBK1768:C0949658:83978005
|CLNHGVS=NC_000014.8:g.23899800A>G; NC_000014.8:g.23899800A>T
|CLNSIG=4
|Disease=AllHighlyPenetrant; Primary familial hypertrophic cardiomyopathy
|FwdALT=A,C
|FwdREF=T
|GENEINFO=MYH7:4625
|GENE_ID=4625
|GENE_NAME=MYH7
|REF=A
|RSPOS=23899800
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=138
|rsid=397516275
}}