rs3745274, CYP2B6

N. diseases: 30
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neurologic Symptoms
CUI: C0235031
Disease: Neurologic Symptoms
0.010 GeneticVariation BEFREE The CYP2B6 G516T genotype was also associated with central nervous system symptoms at week 1 (P = 0.036). 15622315 2004