{{Rsnum
|rsid=116840795
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CAV3
|position=8745580
|Gene_s=CAV3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=116840795
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=8787266
|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.8787266G>A
|CLNORIGIN=0
|CLNSIG=1
|CLNCUI=123320
|CLNDBN=not provided
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000024391.1
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3)
|CLNSRCID=CAV3_00015
|Disease=not provided
}}{{PMID|15099591}} A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia.
{{omim
|id=123320
|rsnum=116840795
}}