{{Rsnum
|rsid=1008642
|Gene=CAV3
|Chromosome=3
|position=8733975
|Orientation=plus
|GMAF=0.3682
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CAV3,SSUH2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 59.3 | 34.5 | 6.2
| HCB | 35.8 | 48.9 | 15.3
| JPT | 43.4 | 47.8 | 8.8
| YRI | 17.7 | 46.9 | 35.4
| ASW | 17.5 | 61.4 | 21.1
| CHB | 35.8 | 48.9 | 15.3
| CHD | 33.0 | 50.5 | 16.5
| GIH | 63.4 | 35.6 | 1.0
| LWK | 18.2 | 46.4 | 35.5
| MEX | 44.8 | 44.8 | 10.3
| MKK | 18.6 | 49.4 | 32.1
| TSI | 43.1 | 45.1 | 11.8
| HapMapRevision=28
}}{{omim
|id=601253
|rsnum=1008642
|variant=0014
}}

{{ClinVar
|rsid=1008642
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=8775661
|CHROM=3
|GMAF=0.3686
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x05017800000017051f110100
|GENEINFO=CAV3:859
|GENE_NAME=CAV3
|GENE_ID=859
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000003.11:g.8775661C>G; NC_000003.11:g.8775661C>T
|CLNORIGIN=0
|CLNSRCID=
CAV3_00038; 601253.0014; 3492; CAV3_00016
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000008786.1; RCV000024392.1; RCV000039807.2
|Tags=PM;TPA;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.6318; 0.3682
|CLNDBN=Distal myopathy, Tateyama type; not provided; AllHighlyPenetrant
|CLNDSDB=MedGen:OMIM; MedGen
|CLNDSDBID=CN118020:614321; CN169374
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant; Emory University
|COMMON=1
|Disease=Distal myopathy; not provided; AllHighlyPenetrant
}}

{{PMID Auto
|PMID=20592870
|Title=Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes.
|OA=1
}}

{{PMID Auto
|PMID=14672715
|Title=Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy.
}}

{{PMID Auto
|PMID=15318349
|Title=Phenotypic variability associated with Arg26Gln mutation in caveolin3.
}}

{{PMID Auto
|PMID=15564037
|Title=Two novel CAV3 gene mutations in Japanese families.
}}

{{PMID Auto
|PMID=15580566
|Title=Molecular and muscle pathology in a series of caveolinopathy patients.
}}

{{PMID Auto
|PMID=17556197
|Title=Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}