{{Rsnum
|rsid=113994176
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GCA)
|geno3=(GCA;GCA)
|Gene=JUP
|position=41771736
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=173325
|rsnum=113994176
|variant=0002
}}{{PMID|17924338|OA=1
}} A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy.{{ClinVar
|ALT=TTGC
|CHROM=17
|CLNACC=RCV000014570.18
|CLNALLE=1
|CLNDBN=Arrhythmogenic right ventricular cardiomyopathy, type 12
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1131:C1969081:611528
|CLNHGVS=NC_000017.10:g.39927989_39927991dupTGC
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1131; 173325.0002
|Disease=Arrhythmogenic right ventricular cardiomyopathy
|FwdALT=GCA
|GENEINFO=JUP:3728
|GENE_ID=3728
|GENE_NAME=JUP
|REF=T
|RSPOS=39927988
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=132
|rsid=113994176
}}