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 		0.900 Biomarker disease GENOMICS_ENGLAND Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257 2017
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 Biomarker disease GENOMICS_ENGLAND SCN5A mutation in Chinese patients with arrhythmogenic right ventricular dysplasia. 24317018 2014
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 GeneticVariation disease UNIPROT MOG1 rescues defective trafficking of Na(v)1.5 mutations in Brugada syndrome and sick sinus syndrome. 23420830 2013
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 Biomarker disease GENOMICS_ENGLAND Concomitant Brugada-like and short QT electrocardiogram linked to SCN5A mutation. 22490985 2012
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 Biomarker disease MGD Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro. 21824921 2011
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 Biomarker disease GENOMICS_ENGLAND The genetics of dilated cardiomyopathy. 20186049 2010
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 GeneticVariation disease UNIPROT SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia. 15466643 2004
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 Biomarker disease GENOMICS_ENGLAND SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. 7889574 1995
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 CausalMutation disease CLINVAR
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 GeneticVariation disease CLINVAR
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.900 Biomarker disease CTD_human