NQO1, NAD(P)H quinone dehydrogenase 1, 1728

N. diseases: 368; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE In the stratified analysis based on cancer types, significant associations were observed between NQO1 C609T polymorphism and GC (OR = 1.38, 95% CI = 1.11-1.72, p = 0.003) and CRC (OR = 1.18, 95% CI = 1.06-1.30, p = 0.001), but not with EC (OR = 1.16, 95% CI = 0.99-1.35, p = 0.06). 29652514 2019
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE Our study shows that individuals carrying the NQO1 C609T variant allele and genotypes are more susceptible to EC. 28203294 2017
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE NQO1 rs1800566 C>T polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population. 24354914 2014
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE Therefore, the meta-analysis suggests that NQO1 Pro187Ser polymorphism is associated with esophageal cancer risk. 24213850 2014
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE Our pooled data suggest a significant association exists between NQO1 C609T polymorphism and EC among Chinese. 24142529 2014
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE Overall, a significant association was found between the NQO1 C609T variant and esophageal cancer under a recessive model (OR = 1.647; 95% CI = 1.233-2.200). 23497461 2013
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE We expand previous studies by showing that the NQO1 gene 609 C>T polymorphism might contribute to EC occurrence, especially in Eastern Asians. 22017531 2012
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE Meta analysis of NQO1 polymorphism also indicated null association of the polymorphism with EC overall or with cancer cases stratified by tumor histopathology/ethnicity. 22770696 2012
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.090 GeneticVariation disease BEFREE NQO1 C609T polymorphism associated with esophageal cancer and gastric cardiac carcinoma in North China. 12854127 2003