Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.700 Biomarker disease GENOMICS_ENGLAND Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation. 26677014 2016
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.700 GeneticVariation disease UNIPROT Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation. 26677014 2016
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.700 GeneticVariation disease UNIPROT Autosomal dominant SCN8A mutation with an unusually mild phenotype. 27210545 2016
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.700 GeneticVariation disease CLINVAR A novel de novo mutation of SCN8A (Nav1.6) with enhanced channel activation in a child with epileptic encephalopathy. 24874546 2014
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.700 Biomarker disease CTD_human
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.700 CausalMutation disease CLINVAR
Entrez Id: 3786
Gene Symbol: KCNQ3
KCNQ3 		0.100 CausalMutation disease CLINVAR