rs121913006, DSG2

N. diseases: 2
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
CUI: C1857777
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.800 GeneticVariation UNIPROT Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations. 21062920 2011
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
CUI: C1857777
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.800 GeneticVariation UNIPROT Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia. 19863551 2010
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
CUI: C1857777
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.800 GeneticVariation UNIPROT Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy. 20031617 2009
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
CUI: C1857777
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.800 GeneticVariation UNIPROT DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy. 16773573 2006
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
CUI: C1857777
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
0.800 CausalMutation CLINVAR