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 		0.110 GeneticVariation disease BEFREE KCNQ2 mutations can present with a neonatal onset multifocal myoclonus-like dyskinesia. 22169383 2012
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.110 Biomarker disease HPO