{{Rsnum
|rsid = 28936685
|Gene = CAV3
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|Chromosome=3
|position=8745671
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAV3,SSUH2
}}{{omim
|desc=RIPPLING MUSCLE DISEASE 2
|id=601253
|rsnum=28936685
|variant=0009
}}
{{ neighbor
| rsid = 28936686
| distance = 17
}}

{{ClinVar
|rsid=28936685
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=8787357
|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.8787357T>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000008779.1; RCV000024387.1
|CLNDBN=Rippling muscle disease 2; not provided
|CLNDSDB=MedGen
|CLNDSDBID=C1832560
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNSRCID=CAV3_00011; 601253.0009
|Disease=Rippling muscle disease 2; not provided
}}

{{PMID|12666119}} Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}