{{Rsnum
|rsid=80338800
|Chromosome=15
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=CAPN3
|position=42387804
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAPN3
}}{{omim
|id=114240
|rsnum=80338800
|variant=0009
}}{{ClinVar
|rsid=80338800
|Reversed=0
|FwdREF=A
|FwdALT=
|REF=CA
|ALT=C
|RSPOS=42680000
|CHROM=15
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=CAPN3:825
|GENE_NAME=CAPN3
|GENE_ID=825
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.42680002delA
|CLNSRC=GTR; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=GTR000330880; NBK1313; 114240.0009
|CLNSIG=5
|CLNCUI=C1869123; C1869123
|CLNDBN=Limb-girdle muscular dystrophy, type 2A; not provided
|Disease=Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000019188.22; RCV000078099.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1313:NBK1408:C1869123:253600:267
}}{{PMID Auto
|PMID=161007
|Title=[Hazards of modern residential and urban areas to child health and development (author's transl)].
}}

{{PMID Auto
|PMID=9266733
|Title=A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.
}}

{{PMID Auto
|PMID=10679950
|Title=High incidence of 550delA mutation of CAPN3 in LGMD2 patients from Russia.
}}

{{PMID Auto
|PMID=14981715
|Title=Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia.
}}

{{PMID Auto
|PMID=15725583
|Title=The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.
}}

{{PMID Auto
|PMID=17318636
|Title=A large deletion and novel point mutations in the calpain 3 gene (CAPN3) in Bulgarian LGMD2A patients.
}}