Gene: GRIN2A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2903
Gene Symbol: GRIN2A
GRIN2A 		0.010 GeneticVariation disease BEFREE Two unrelated individuals with epileptic encephalopathy carry a de novo variant in the gene encoding the GluN2A NMDA receptor subunit: a N615K missense variant in the M2 pore helix (GRIN2A<sup>C1845A</sup> ). 30604514 2019