{{Rsnum
|rsid=28928909
|Gene=MYF6
|Chromosome=12
|position=80708053
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=MYF6
}}{{omim
|desc=MYOPATHY, CENTRONUCLEAR, MILD
|id=159991
|rsnum=28928909
|variant=0001
}}

{{ClinVar
|rsid=28928909
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=81101832
|CHROM=12
|GMAF=0.0009
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=MYF6:4618
|GENE_NAME=MYF6
|GENE_ID=4618
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.81101832G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=159991.0001
|CLNSIG=5
|CLNCUI=CN119609
|CLNDBN=Myopathy, centronuclear, 3
|Disease=Myopathy
|CLNACC=RCV000015216.24
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280703:614408:169189
|COMMON=0
}}

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