{{Rsnum
|rsid = 28937597
|Gene = MYOT
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=5
|position=137870821
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC101928005,MYOT
}}{{omim
|desc=MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1A
|id=604103
|rsnum=28937597
|variant=0001
}}

{{ neighbor
| rsid = 6890689
| distance = 50
}}

{{ClinVar
|rsid=28937597
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=137206510
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=MYOT:9499
|GENE_NAME=MYOT
|GENE_ID=9499
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.137206510C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1499; 604103.0001
|CLNSIG=5
|CLNCUI=C1834659
|CLNDBN=Limb-girdle muscular dystrophy, type 1A
|Disease=Limb-girdle muscular dystrophy
|CLNACC=RCV000006190.2
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1408:NBK1499:C1834659:159000:266
}}

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