GABRA1: epileptic encephalopathy, early infantile, 19 (MIM 615744); possible susceptibility allele; juvenile myoclonic epilepsy (MIM 611136) and childhood absence epilepsy (MIM 611136);GABRA6: possible susceptibility allele for childhood absence epilepsy (Table S2). The gene discussed is GABRA6; the disease is juvenile myoclonic epilepsy.