rs211037, GABRG2

N. diseases: 14
Disease: Symptomatic epilepsy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Symptomatic epilepsy
CUI: C1406659
Disease: Symptomatic epilepsy
0.010 GeneticVariation BEFREE The rs211037-rs210987 and rs2422106-rs211014-rs401750 haplotypes we</span>re also associated with susceptibility to SE in Chinese. 26452361 2016