{{Rsnum
|rsid=116840805
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CAV3
|position=8745725
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAV3,SSUH2
}}{{omim
|id=601253
|rsnum=116840805
|variant=0001
}}{{ClinVar
|rsid=116840805
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=8787411
|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.8787411C>T
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=CAV3_00001; 601253.0001
|CLNSIG=5
|CLNCUI=C1832567
|CLNDBN=Limb-girdle muscular dystrophy, type 1C; Rippling muscle disease 2; not provided
|Disease=Limb-girdle muscular dystrophy; Rippling muscle disease 2; not provided
|CLNACC=RCV000008765.3; RCV000008766.2; RCV000024379.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1385:C1832567:607801:265; C1832560
}}{{PMID Auto
|PMID=9537420
|Title=Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy.
}}

{{PMID Auto
|PMID=11431690
|Title=Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease.
}}