{{Rsnum
|rsid=121913012
|Chromosome=18
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DSG2
|position=31524865
|Gene_s=DSG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=125671
|rsnum=121913012
|variant=0007
}}{{ClinVar
|rsid=121913012
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=29104828
|CHROM=18
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=DSG2:1829
|GENE_NAME=DSG2
|GENE_ID=1829
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.29104828G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=125671.0007
|CLNSIG=5
|CLNCUI=C1857777
|CLNDBN=Arrhythmogenic right ventricular cardiomyopathy, type 10; Arrhythmogenic right ventricular cardiomyopathy
|Disease=Arrhythmogenic right ventricular cardiomyopathy; Arrhythmogenic right ventricular cardiomyopathy
|CLNACC=RCV000018309.26; RCV000029673.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1131:C1857777:610193; NBK1131:C0349788:253528005:281170005
}}{{PMID Auto
|PMID=16505173
|Title=Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy.
}}

{{PMID Auto
|PMID=18007692
|Title=Genetic diseases of junctions.
}}

{{PMID Auto
|PMID=18382419
|Title=Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
|OA=1
}}

{{PMID Auto
|PMID=20847325
|Title=The cardiac desmosome and arrhythmogenic cardiomyopathies: from gene to disease.
}}