rs2231142, ABCG2

N. diseases: 56
Disease: Epilepsy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.020 GeneticVariation BEFREE Interaction between ABCG2 421C>A polymorphism and valproate in their effects on steady-state disposition of lamotrigine in adults with epilepsy. 29791014 2018
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.020 GeneticVariation BEFREE These results suggested that the polymorphisms of OCT1 rs628031 and ABCG2 rs2231142 may affect LTG metabolism in Chinese patients with epilepsy. 27610747 2016