Gene: SCN2A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A 		0.300 Biomarker disease CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A 		0.300 Biomarker disease CTD_human Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. 23708187 2013
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A 		0.300 Biomarker disease CTD_human Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2. 16464983 2006