Gene: SCN5A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.030 GeneticVariation disease BEFREE We report on the genetic status of BrS patients of Greek origin amongst whom novel SCN5A mutations were a frequent underlying cause of the syndrome. 19406494 2010
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.030 GeneticVariation disease BEFREE In 20% of cases, the syndrome is associated with mutations of the cardiac sodium channel gene SCN5A. 16138883 2005
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.030 GeneticVariation disease BEFREE The effect of intravenous ajmaline (1 mg/kg), procainamide (10 mg/kg), or flecainide (2 mg/kg) on the ECG was studied in 34 patients with the syndrome and transient normalization of the ECG (group A), 11 members of 3 families in whom a SCN5A mutation was associated with the syndrome and 8 members in whom it was not (group B), and 53 control subjects (group C). 10662748 2000