{{Rsnum
|rsid=267606908
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYH7
|position=23424112
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=14
|CLNACC=RCV000015185.24; RCV000035817.1
|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.23893321T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=160760.0039
|Disease=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|FwdALT=G
|FwdREF=A
|GENEINFO=MYH7:4625
|GENE_ID=4625
|GENE_NAME=MYH7
|REF=T
|RSPOS=23893321
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606908
}}