Gene: SCN1B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6324
Gene Symbol: SCN1B
SCN1B 		0.020 GeneticVariation disease BEFREE We screened for mutations in the genes encoding the 5 sodium β subunits (SCN1B isoforms a and b, SCN2B, SCN3B, and SCN4B) from 30 nonrelated patients who were clinically diagnosed with LQTS without mutations in common LQTS-related genes. 24662403 2014
Entrez Id: 6324
Gene Symbol: SCN1B
SCN1B 		0.020 Biomarker disease BEFREE Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of long QT syndrome. 18052691 2008