rs211037, GABRG2

N. diseases: 14
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
0.050 GeneticVariation BEFREE GABRG2 rs211037 TT homozygotes and T allele variants have an increased risk for developing febrile seizures.</span> 29379546 2018
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
0.050 GeneticVariation BEFREE In conclusion, rs211037 alone may be a risk factor for FS, partial seizure, and SE, and in linkage disequilibrium with rs210987 can contribute to FS and SE in Asians, particularly in Chinese. 26452361 2016
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
0.050 GeneticVariation BEFREE GABRG2, rs211037 is associated with epilepsy susceptibility, but not with antiepileptic drug resistance and febrile seizures. 24061200 2013
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
0.050 GeneticVariation BEFREE This study showed significant association of GABRG2 rs211037 with susceptibility to FS, caused by two studies with small sample sizes, however the possibility of false positive results due to the effect of significant studies for FS cannot be excluded. 23140995 2013
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
0.050 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