rs211037, GABRG2

N. diseases: 14
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Seizures
CUI: C0036572
Disease: Seizures
0.040 GeneticVariation BEFREE The GABRG2 588 C > T polymorphism may decrease the duration of seizures in JME patients. 29785705 2018
Seizures
CUI: C0036572
Disease: Seizures
0.040 GeneticVariation BEFREE A significant association was found with the TT homozygous genotype and T allele for both febrile seizures and epilepsy for the C588T locus, while GABRG2 G>A 3145 showed no significant association with any type of seizure. 29379546 2018
Seizures
CUI: C0036572
Disease: Seizures
0.040 GeneticVariation BEFREE One hundred twenty-seven cases of seizure (86 GS and 41 FS) patients were analyzed for MDR1 C3435T and GABRG2 C588T gene polymorphisms using restriction fragment length polymorphism-polymerase chain reaction.Serum PHT levels were analyzed. 22239287 2012
Seizures
CUI: C0036572
Disease: Seizures
0.040 GeneticVariation BEFREE The aim of our study was to find out the possible role of single nucleotide polymorphisms (SNPs) present in GABRA1 IVS11+15 A>G (rs2279020) and GABRG2 588C>T (rs211037) genes in seizure susceptibility and pharmaco-resistance in northern Indian patients with epilepsy. 20356767 2010