Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.510 Biomarker CLINGEN Mutations in SCN2B, encoding voltage-gated sodium channel β2-subunits, are associated with human cardiac arrhythmias, including atrial fibrillation and Brugada syndrome. 27932425

2016
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.510 Biomarker CLINGEN Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome. 26179811

2015
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.510 Biomarker CLINGEN Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort. 26173111

2015
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.510 Biomarker CLINGEN The effect of the mutant β2 subunit on the INa strongly suggests that SCN2B is a new candidate gene associated with BrS. 23559163

2013
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.510 Biomarker CLINGEN Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477

2009