Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57468
Gene Symbol: SLC12A5
SLC12A5 		0.700 Biomarker disease GENOMICS_ENGLAND Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delay. 27436767 2016
Entrez Id: 57468
Gene Symbol: SLC12A5
SLC12A5 		0.700 GeneticVariation disease UNIPROT Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures. 26333769 2015
Entrez Id: 57468
Gene Symbol: SLC12A5
SLC12A5 		0.700 Biomarker disease CTD_human
Entrez Id: 57468
Gene Symbol: SLC12A5
SLC12A5 		0.700 CausalMutation disease CLINVAR
Entrez Id: 57468
Gene Symbol: SLC12A5
SLC12A5 		0.700 GeneticVariation disease CLINVAR