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 		0.130 GeneticVariation phenotype LHGDN Functionally significant mutations and rare variants in SCN5A may contribute to SCD risk among women. 18071069 2008
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.130 GeneticVariation phenotype LHGDN This suggests that genetic determinants located in KCNQ1, KCNE1, KCNH2 and SCN5A influence QTc length in healthy individuals and may represent risk factors for arrhythmias or cardiac sudden death in patients with cardiovascular diseases. 16132053 2005
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.130 GeneticVariation phenotype LHGDN Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks. 16061744 2005
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.130 Biomarker phenotype HPO