rs201934979, CYP1A2

N. diseases: 3
Disease: Tardive Dyskinesia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Tardive Dyskinesia
CUI: C0686347
Disease: Tardive Dyskinesia
0.010 GeneticVariation BEFREE No significant differences in genotypes frequencies of the CYP2D6 C100T polymorphism were observed between patients with TD and without TD (Chi2=4.078, P>0.05), but patients with TD had a significant excess of the T allele compared with those without TD (Chi2=4.28, P<0.05). 16490169 2006