Gene: SCN8A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.600 Biomarker disease GENOMICS_ENGLAND Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation. 26677014 2016
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.600 Biomarker disease GENOMICS_ENGLAND De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP. 22365152 2012
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.600 CausalMutation disease CLINVAR
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.600 Biomarker disease CTD_human