Disease: Epilepsy, Rolandic ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1250662891
rs1250662891
Entrez Id: 2903
Gene Symbol: GRIN2A
GRIN2A
CUI: C0376532
Disease:
Epilepsy, Rolandic 		C 0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018