{{Rsnum
|rsid=121908959
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DYSF
|position=71674242
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DYSF
}}{{omim
|id=603009
|rsnum=121908959
|variant=0012
}}{{ClinVar
|rsid=121908959
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=71901372
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=DYSF:8291
|GENE_NAME=DYSF
|GENE_ID=8291
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.71901372C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=7732; 603009.0012
|CLNSIG=5
|CLNCUI=C1850808; C1847532; C1850889
|CLNDBN=Miyoshi myopathy; Myopathy, distal, with anterior tibial onset; Limb-girdle muscular dystrophy, type 2B; not provided
|Disease=Miyoshi myopathy; Myopathy; Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000007061.1; RCV000007062.1; RCV000007063.1; RCV000080312.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1303:C1850808:254130:45448; C1847532:606768; NBK1303:NBK1408:C1850889:253601:268
}}