{{Rsnum
|rsid = 28933098
|Gene = MYH7
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=14
|position=23415021
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH7
}}{{omim
|desc=MYOPATHY, MYOSIN STORAGE
|id=160760
|rsnum=28933098
|variant=0028
}}

{{ClinVar
|rsid=28933098
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=23884230
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MYH7:4625
|GENE_NAME=MYH7
|GENE_ID=4625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.23884230G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160760.0028
|CLNSIG=5
|CLNCUI=C1842160; CN074265
|CLNDBN=Myopathy, myosin storage; Scapuloperoneal myopathy, MYH7-related
|Disease=Myopathy; Scapuloperoneal myopathy
|CLNACC=RCV000015170.24; RCV000015171.20
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1842160:608358; CN074265:181430
}}

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