{{Rsnum
|rsid=121909280
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CAV3
|position=8745602
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAV3,SSUH2
}}{{omim
|id=601253
|rsnum=121909280
|variant=0013
}}{{ClinVar
|rsid=121909280
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=8787288
|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.8787288C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000008785.2; RCV000024395.1
|CLNDBN=Cardiomyopathy, familial hypertrophic; not provided
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNSRCID=CAV3_00019; 601253.0013
|Disease=Cardiomyopathy; not provided
}}{{PMID Auto
|PMID=14672715
|Title=Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy.
}}