{{Rsnum
|rsid=121908956
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=DYSF
|position=71564074
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DYSF
}}{{omim
|id=603009
|rsnum=121908956
|variant=0007
}}{{ClinVar
|rsid=121908956
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=71791204
|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.71791204C>G
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=15732; 603009.0007
|CLNSIG=5
|CLNCUI=C1850889; C1850808
|CLNDBN=Limb-girdle muscular dystrophy, type 2B; Miyoshi myopathy; not provided
|Disease=Limb-girdle muscular dystrophy; Miyoshi myopathy; not provided
|CLNACC=RCV000007055.1; RCV000007056.1; RCV000080252.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1303:NBK1408:C1850889:253601:268; NBK1303:C1850808:254130:45448
}}