Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 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: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 GeneticVariation disease UNIPROT Epileptic encephalopathy de novo GABRB mutations impair γ-aminobutyric acid type A receptor function. 26950270 2016
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 GeneticVariation disease UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267 2016
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 GeneticVariation disease UNIPROT De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies. 27476654 2016
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 GeneticVariation disease UNIPROT De novo mutations in moderate or severe intellectual disability. 25356899 2014
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 GeneticVariation disease UNIPROT De novo mutations in epileptic encephalopathies. 23934111 2013
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 CausalMutation disease CLINVAR
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3 		0.600 Biomarker disease CTD_human