rs1258159645, NQO1

N. diseases: 37
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
0.030 GeneticVariation BEFREE Neither the NQO1 Pro187Ser nor the SOD2 Ala9Val appear to play a major role in TD risk, although additional polymorphisms should be tested before the role of NQO1 and SOD2 in TD can be completely excluded. 19778569 2010
Tardive Dyskinesia
CUI: C0686347
Disease: Tardive Dyskinesia
0.030 GeneticVariation BEFREE The combined genotypes of T/T in NQO1 Pro187Ser and Val/Val in MnSOD Ala-9Val polymorphisms were found to be independently associated with a significantly higher risk of TD. 18977034 2008
Tardive Dyskinesia
CUI: C0686347
Disease: Tardive Dyskinesia
0.030 GeneticVariation BEFREE (2004) reported a significant association between the Pro187Ser polymorphism in the NQO1 gene and TD. 16775388 2006