SLC22A2, solute carrier family 22 member 2, 6582

N. diseases: 98; N. variants: 16
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0150055
Disease: Chronic pain
Chronic pain
0.010 GeneticVariation phenotype BEFREE Pharmacogenetics-based population pharmacokinetic analysis of gabapentin in patients with chronic pain: Effect of OCT2 and OCTN1 gene polymorphisms. 30192429 2019