{{Rsnum
|rsid=199476331
|Chromosome=3
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CACCTTCAC)
|geno3=(CACCTTCAC;CACCTTCAC)
|Gene=CAV3
|position=8745600
|Gene_s=CAV3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199476331
|Reversed=0
|FwdREF=CACCTTCAC
|FwdALT=
|REF=CCACCTTCAC
|ALT=C
|RSPOS=8787285
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.8787286_8787294delCACCTTCAC
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=CAV3_00002; 601253.0002
|CLNSIG=5
|CLNCUI=C1832567; C1832567
|CLNDBN=Limb-girdle muscular dystrophy, type 1C; not provided
|Disease=Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000008767.2; RCV000024380.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1385:C1832567:607801:265
|GENEINFO=CAV3:859
|GENE_ID=859
|GENE_NAME=CAV3
}}{{PMID Auto
|PMID=9537420
|Title=Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy.
}}

{{PMID Auto
|PMID=14600260
|Title=A caveolin-3 mutant that causes limb girdle muscular dystrophy type 1C disrupts Src localization and activity and induces apoptosis in skeletal myotubes.
}}