{{Rsnum
|rsid=116840787
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CAV3
|position=8733992
|Gene_s=CAV3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=116840787
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=8775678
|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.8775678T>C
|CLNORIGIN=1
|CLNSIG=1
|CLNCUI=607801
|CLNDBN=not provided
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000024426.1
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3)
|CLNSRCID=CAV3_00051
|Disease=not provided
}}{{PMID Auto
|PMID=16730439
|Title=Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy.
}}

{{PMID Auto
|PMID=21294223
|Title=Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle.
|OA=1
}}
{{omim
|id=607801
|rsnum=116840787
}}