{{Rsnum
|rsid=121908954
|Gene=DYSF
|Chromosome=2
|position=71602794
|Orientation=plus
|GMAF=0.002296
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=DYSF
}}{{omim
|id=603009
|rsnum=121908954
|variant=0003
}}{{ClinVar
|rsid=121908954
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=71829924
|CHROM=2
|GMAF=0.0023
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=DYSF:8291
|GENE_NAME=DYSF
|GENE_ID=8291
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.71829924A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603009.0003
|CLNSIG=5
|CLNCUI=C1850808; C1850889
|CLNDBN=Miyoshi myopathy; Limb-girdle muscular dystrophy, type 2B
|Disease=Miyoshi myopathy; Limb-girdle muscular dystrophy
|CLNACC=RCV000007049.1; RCV000007050.1
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9977; 0.002296
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1303:C1850808:254130:45448; NBK1303:NBK1408:C1850889:253601:268
|COMMON=0
}}