{{Rsnum
|rsid=267606911
|Chromosome=14
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYH7
|position=23428587
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=14
|CLNACC=RCV000015184.24; RCV000035727.1
|CLNALLE=1
|CLNDBN=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1385:NBK1768:CN030093:192600; NBK1768:C0949658:83978005
|CLNHGVS=NC_000014.8:g.23897796C>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=160760.0038
|Disease=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|FwdALT=T
|FwdREF=G
|GENEINFO=MYH7:4625
|GENE_ID=4625
|GENE_NAME=MYH7
|REF=C
|RSPOS=23897796
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606911
}}