{{Rsnum
|rsid=116840776
|Gene=CAV3
|Chromosome=3
|position=8745627
|Orientation=plus
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=CAV3,SSUH2
}}{{omim
|id=601253
|rsnum=116840776
|variant=0004
}}{{ClinVar
|rsid=116840776
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=8787313
|CHROM=3
|GMAF=0.0018
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000040016110100
|GENEINFO=CAV3:859
|GENE_NAME=CAV3
|GENE_ID=859
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.8787313C>G
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=CAV3_00004; 601253.0004
|CLNSIG=5
|CLNCUI=C1832567
|CLNDBN=Limb-girdle muscular dystrophy, type 1C; not provided
|Disease=Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000008769.1; RCV000024381.1
|Tags=PM;PMC;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1385:C1832567:607801:265
|COMMON=0
}}{{PMID|9536092}} Caveolin-3 in muscular dystrophy.

{{PMID|11251997}} Mutations in the caveolin-3 gene: When are they pathogenic?

{{PMID|9536092}} Caveolin-3 in muscular dystrophy.

{{PMID|11251997}} Mutations in the caveolin-3 gene: When are they pathogenic?

{{PMID|17060380}} Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome.

{{PMID|17210839}} Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.