Disease: Epilepsy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs796052549
rs796052549
Entrez Id: 2903;105371077
Gene Symbol: GRIN2A;LOC105371077
GRIN2A;LOC105371077
CUI: C0014544
Disease:
Epilepsy 		0.010 GeneticVariation BEFREE We identified one de novo missense GRIN2A mutation (Asp731Asn, GluN2A(D731N)) in a child with unexplained epilepsy and DD. 28182669 2017