Gene: KCNQ2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.300 Biomarker phenotype CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.300 Biomarker phenotype CTD_human Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2. 16464983 2006