rs211037, GABRG2

N. diseases: 14
Disease: Absence Epilepsy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Absence Epilepsy
CUI: C0014553
Disease: Absence Epilepsy
0.010 GeneticVariation BEFREE The association study did not find any significant differences in the allele and genotype frequencies of the common exon 5 polymorphism (C588T) between patients with idiopathic absence epilepsy and controls (P>.35). 12117362 2002