{{Rsnum
|rsid=267606910
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYH7
|position=23431589
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000015186.24; RCV000015187.24
|CLNALLE=1
|CLNDBN=Familial hypertrophic cardiomyopathy 1; Left ventricular noncompaction 5
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=NBK1385:NBK1768:CN030093:192600; C3150690
|CLNHGVS=NC_000014.8:g.23900798C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=160760.0040
|Disease=Familial hypertrophic cardiomyopathy 1; Left ventricular noncompaction 5
|FwdALT=A
|FwdREF=G
|GENEINFO=MYH7:4625
|GENE_ID=4625
|GENE_NAME=MYH7
|REF=C
|RSPOS=23900798
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606910
}}