Gene: KCNQ3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3786
Gene Symbol: KCNQ3
KCNQ3 		0.100 CausalMutation phenotype CLINVAR De novo mutations in epileptic encephalopathies. 23934111 2013
Entrez Id: 3786
Gene Symbol: KCNQ3
KCNQ3 		0.100 CausalMutation phenotype CLINVAR Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. 23020937 2012