{{Rsnum
|rsid=121909282
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CAV3
|position=8745647
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAV3,SSUH2
}}{{omim
|id=601253
|rsnum=121909282
|variant=0021
}}{{ClinVar
|rsid=121909282
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=8787333
|CHROM=3
|dbSNPBuildID=133
|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.8787333T>G
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=CAV3_00059; 601253.0021
|CLNSIG=5
|CLNCUI=C2678485
|CLNDBN=Long QT syndrome 9; not provided
|Disease=Long QT syndrome 9; not provided
|CLNACC=RCV000008794.1; RCV000024434.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C2678485:611818:101016
}}{{PMID Auto
|PMID=17275750
|Title=Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.
|OA=1
}}