{{Rsnum
|rsid=80338803
|Chromosome=15
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=CAPN3
|position=42405938
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAPN3
}}{{omim
|id=114240
|rsnum=80338803
|variant=0008
}}{{ClinVar
|rsid=80338803
|Reversed=0
|FwdREF=GAC
|FwdALT=A
|REF=G
|ALT=GA
|RSPOS=42698129
|CHROM=15
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.42698136_42698137insA
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1313; 114240.0008
|CLNSIG=5
|CLNCUI=C1869123; C1869123
|CLNDBN=Limb-girdle muscular dystrophy, type 2A
|Disease=Limb-girdle muscular dystrophy
|CLNACC=RCV000019187.22
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1313:NBK1408:C1869123:253600:267
|GENEINFO=CAPN3:825
|GENE_ID=825
|GENE_NAME=CAPN3
}}{{PMID Auto
|PMID=9771675
|Title=Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families.
}}

{{PMID Auto
|PMID=11525884
|Title=Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy.
}}