Gene: SCN3B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55800
Gene Symbol: SCN3B
SCN3B 		0.010 GeneticVariation disease BEFREE Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation. 20042427 2010