Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.700 GeneticVariation disease UNIPROT Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes. 27864847 2017
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.700 GeneticVariation disease UNIPROT Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains. 27839871 2016
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.700 CausalMutation disease CLINVAR Utility of Whole Exome Sequencing for Genetic Diagnosis of Previously Undiagnosed Pediatric Neurology Patients. 27572814 2016
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.700 GeneticVariation disease UNIPROT GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy. 24272827 2014
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.700 Biomarker disease CTD_human
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.700 GeneticVariation disease CLINVAR