Gene: GRIN2B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.110 GeneticVariation phenotype BEFREE We identified GRIN2B gain-of-function mutations as a cause of West syndrome with severe developmental delay as well as of ID with childhood onset focal epilepsy. 24272827 2014
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.110 GeneticVariation phenotype CLINVAR