Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55800
Gene Symbol: SCN3B
SCN3B
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7
0.900 GeneticVariation UNIPROT Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation. 21051419

2011

Entrez Id: 55800
Gene Symbol: SCN3B
SCN3B
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7
0.900 GeneticVariation UNIPROT Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population. 20558140

2010

Entrez Id: 55800
Gene Symbol: SCN3B
SCN3B
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7
0.900 GeneticVariation UNIPROT A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype. 20031595

2009