Mutations in GABRG2 are associated with febrile seizures (FS) and various genetic epilepsy syndromes, which suggests a broad range of phenotypical spectrum associated with GABRG2 variants (Kang and Macdonald, 2016). The gene discussed is GABRG2; the disease is Febrile seizure (within the age range of 3 months to 6 years).