{{Rsnum
|rsid=116840782
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CAV3
|position=8733960
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAV3,SSUH2
}}{{omim
|id=601253
|rsnum=116840782
|variant=0008
}}{{ClinVar
|rsid=116840782
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=8775646
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=CAV3:859
|GENE_NAME=CAV3
|GENE_ID=859
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.8775646C>A
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=CAV3_00010; 601253.0008
|CLNSIG=5
|CLNCUI=C1832567
|CLNDBN=Rippling muscle disease 2; Limb-girdle muscular dystrophy, type 1C; not provided
|Disease=Rippling muscle disease 2; Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000008770.1; RCV000008771.2; RCV000024386.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1832560; NBK1385:C1832567:607801:265
}}{{PMID|12557291}} Consequences of a novel caveolin-3 mutation in a large German family.

{{PMID|19835634|OA=1
}} Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes.

{{PMID|21294223|OA=1
}} Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle.