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 phenotype BEFREE Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H. 28139826 2017
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.110 Biomarker phenotype HPO