Gene: CLCN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.020 GeneticVariation disease BEFREE De novo SCN1A, SCN8A, and CLCN2 mutations in childhood absence epilepsy. 31054517 2019
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.020 GeneticVariation disease BEFREE We conclude that CLCN2 may be a susceptibility locus in a subset of cases of childhood absence epilepsy. 17580110 2007