{{Rsnum
|rsid=121909281
|Gene=CAV3
|Chromosome=3
|position=8733916
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=CAV3,SSUH2
}}{{omim
|id=601253
|rsnum=121909281
|variant=0020
}}{{ClinVar
|rsid=121909281
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=8775602
|CHROM=3
|GMAF=0.0014
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000040016110100
|GENEINFO=CAV3:859
|GENE_NAME=CAV3
|GENE_ID=859
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000003.11:g.8775602G>C
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=CAV3_00058; 601253.0020
|CLNSIG=5
|CLNCUI=C2678485
|CLNDBN=Long QT syndrome 9; not provided
|Disease=Long QT syndrome 9; not provided
|CLNACC=RCV000008793.1; RCV000024433.1
|Tags=PM;PMC;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377; .
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C2678485:611818:101016
|COMMON=1
}}{{PMID Auto
|PMID=17275750
|Title=Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.
|OA=1
}}