{{Rsnum
|rsid=387906882
|Chromosome=5
|position=137870668
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYOT
|Gene_s=MYOT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=5
|CLNACC=RCV000023360.2
|CLNALLE=1
|CLNDBN=Limb-girdle muscular dystrophy, type 1A
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1408:NBK1499:C1834659:159000:266
|CLNHGVS=NC_000005.9:g.137206357G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604103.0007
|Disease=Limb-girdle muscular dystrophy
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=137206357
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906882
|GENEINFO=MYOT:9499
|GENE_ID=9499
|GENE_NAME=MYOT
}}