rs368299411, DSC2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
CUI: C1864850
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
0.700 GeneticVariation UNIPROT Whole-Exome Sequencing Identifies a Novel Mutation of Desmocollin 2 in a Chinese Family With Arrhythmogenic Right Ventricular Cardiomyopathy. 28256248 2017
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
CUI: C1864850
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
0.700 GeneticVariation UNIPROT Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations. 21062920 2011
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
CUI: C1864850
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
0.700 GeneticVariation UNIPROT Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia. 19863551 2010
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
CUI: C1864850
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
0.700 GeneticVariation UNIPROT Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2. 17033975 2006