{{Rsnum
|rsid=121908457
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYOT
|position=137870815
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC101928005,MYOT
}}{{omim
|id=604103
|rsnum=121908457
|variant=0002
}}{{ClinVar
|rsid=121908457
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=137206504
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MYOT:9499
|GENE_NAME=MYOT
|GENE_ID=9499
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.137206504C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604103.0002
|CLNSIG=5
|CLNCUI=C1834659; C1836607
|CLNDBN=Limb-girdle muscular dystrophy, type 1A; Myotilinopathy
|Disease=Limb-girdle muscular dystrophy; Myotilinopathy
|CLNACC=RCV000006191.3; RCV000054443.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1408:NBK1499:C1834659:159000:266; NBK1499:C1836607:609200
}}