{{Rsnum
|rsid=141764279
|Chromosome=14
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYH7
|position=23418398
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=141764279
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=23887607
|CHROM=14
|dbSNPBuildID=134
|SSR=0
|SAO=1
|VP=0x050068000000040002100100
|GENEINFO=MYH7:4625; MIR208B:100126336
|GENE_NAME=MYH7; MIR208B
|GENE_ID=4625; 100126336
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.23887607G>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|Disease=Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|Tags=PM;PMC;VLD;OTHERKG;LSD
|CLNACC=RCV000030319.1; RCV000035878.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1768:C0949658:83978005; CN169374
}}{{PMID Auto
|PMID=15483641
|Title=One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region.
}}

{{PMID Auto
|PMID=21310275
|Title=Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
|OA=1
}}