rs397514737, GABRG2

N. diseases: 4
Disease: Epilepsy, Rolandic ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Epilepsy, Rolandic
CUI: C0376532
Disease: Epilepsy, Rolandic
0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018