{{Rsnum
|rsid = 3218714
|Gene = MYH7
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=14
|position=23429279
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH7
}}[[Familial hypertrophic cardiomyopathy]]

see also OMIM [http://omim.org/entry/160760#0015 160760.0015]

{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1
|id=160760
|rsnum=3218714
|variant=0015
}}

{{ClinVar
|rsid=3218714
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=23898488
|CHROM=14
|dbSNPBuildID=106
|SSR=0
|SAO=1
|VP=0x050260000000000103110100
|GENEINFO=MYH7:4625
|GENE_NAME=MYH7
|GENE_ID=4625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.23898488G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160760.0015
|CLNSIG=5
|CLNCUI=CN030093
|CLNDBN=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|Disease=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000015158.20; RCV000035707.1
|Tags=RV;PM;S3D;GNO;OTHERKG;PH3;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1385:NBK1768:CN030093:192600; NBK1768:C0949658:83978005
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}