Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.410 CausalMutation CLINVAR Identification of six novel SCN5A mutations in Japanese patients with Brugada syndrome. 21321465

2011
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.410 GeneticVariation CLINVAR A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease. 20564468

2010
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.410 CausalMutation CLINVAR Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families. 18508782

2008
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.410 CausalMutation CLINVAR Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing. 15840476

2005
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.410 CausalMutation 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
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.410 CausalMutation CLINVAR Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel. 10377081

1999