Gene: SCN5A ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.200 CausalMutation disease CLINVAR High prevalence of the SCN5A E1784K mutation in school children with long QT syndrome living on the Okinawa islands. 24871449 2014
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.200 GeneticVariation disease CLINVAR Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. 23631430 2013
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.200 CausalMutation disease CLINVAR Identification of six novel SCN5A mutations in Japanese patients with Brugada syndrome. 21321465 2011
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.200 CausalMutation disease CLINVAR The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome. 18451998 2008
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.200 CausalMutation disease CLINVAR Gene sequencing in neonates and infants with the long QT syndrome. 16379539 2005
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.200 CausalMutation disease CLINVAR Natural history of Brugada syndrome: insights for risk stratification and management. 11901046 2002
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.200 CausalMutation disease CLINVAR Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes. 10727653 2000
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.200 CausalMutation disease CLINVAR Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel. 10377081 1999