{{Rsnum
|rsid = 3218713
|Gene = MYH7
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=14
|position=23431468
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH7
}}[[Familial hypertrophic cardiomyopathy]]

see also OMIM [http://omim.org/entry/160760#0002 160760.0002]

{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| 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=3218713
|variant=0002
}}

{{ClinVar
|rsid=3218713
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=23900677
|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.23900677C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160760.0002
|CLNSIG=5
|CLNCUI=CN030093
|CLNDBN=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|Disease=Familial hypertrophic cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000015144.24; RCV000036000.1
|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}}