{{Rsnum
|rsid=199476335
|Chromosome=3
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TCT)
|geno3=(TCT;TCT)
|Gene=CAV3
|position=8745701
|Gene_s=CAV3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199476335
|Reversed=0
|FwdREF=TCT
|FwdALT=
|REF=TTCT
|ALT=T
|RSPOS=8787386
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.8787387_8787389delTCT
|CLNSRC=Leiden Muscular Dystrophy pages (CAV3); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=CAV3_00014; 601253.0011
|CLNSIG=5
|CLNCUI=C0241005; C0241005; C1832567; C1832567
|CLNDBN=Creatine phosphokinase, elevated serum; Rippling muscle disease 2; Limb-girdle muscular dystrophy, type 1C; not provided
|Disease=Creatine phosphokinase; Rippling muscle disease 2; Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000008781.1; RCV000008782.2; RCV000008783.1; RCV000024390.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1385:C0241005:123320; C1832560; NBK1385:C1832567:607801:265
|GENEINFO=CAV3:859
|GENE_ID=859
|GENE_NAME=CAV3
}}{{PMID Auto
|PMID=14663034
|Title=A CAV3 microdeletion differentially affects skeletal muscle and myocardium.
}}

{{PMID Auto
|PMID=17994539
|Title=Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients.
}}