Variant: rs1060501889 

    present in Gene: GABRG2
    present in Chromosome: 5
    Position on Chromosome: 162149210
    Alleles of this Variant: G/-

rs1060501889 in GABRG2 gene and EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 PMID 27066572 2015 Novel GABRG2 mutations cause familial febrile seizures.

PMID 23720301 2013 Trafficking-deficient mutant GABRG2 subunit amount may modify epilepsy phenotype.

PMID 18566737 2008 SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.

rs1060501889 in GABRG2 gene and FEBRILE CONVULSIONS, FAMILIAL, 8 PMID 18566737 2008 SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.

PMID 27066572 2015 Novel GABRG2 mutations cause familial febrile seizures.

PMID 23720301 2013 Trafficking-deficient mutant GABRG2 subunit amount may modify epilepsy phenotype.