{{Rsnum
|rsid=104893713
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CAV3
|position=8745834
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAV3,SSUH2
}}{{omim
|id=601253
|rsnum=104893713
|variant=0016
}}{{ClinVar
|rsid=104893713
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=8787520
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=3
|VP=0x050168000000000002110100
|GENEINFO=CAV3:859
|GENE_NAME=CAV3
|GENE_ID=859
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.8787520C>G
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=CAV3_00057; 601253.0016
|CLNSIG=5
|CLNCUI=C2678485
|CLNDBN=Long QT syndrome 9; not provided
|Disease=Long QT syndrome 9; not provided
|CLNACC=RCV000008788.2; RCV000024432.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C2678485:611818:101016
}}{{PMID Auto
|PMID=17060380
|Title=Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome.
}}