Disease: Brugada Syndrome (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777023
rs587777023
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.010 GeneticVariation BEFREE In this work, we identified a novel missense mutation (p.Asp211Gly) in the sodium β2 subunit encoded by SCN2B, in a woman diagnosed with BrS. 23559163 2013