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 		0.310 GeneticVariation phenotype BEFREE KCNQ2 mutation in an infant with encephalopathy of infancy with migrating focal seizures. 30530441 2018
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.310 Biomarker phenotype CTD_human KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients. 27602407 2016