Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
0.080 | GeneticVariation | disease | BEFREE | The current meta-analysis suggests no evidence of association between the EPHX1 polymorphism and EC risk. | 25714851 | 2015 | ||||
|
0.080 | GeneticVariation | disease | BEFREE | This study aimed to identify the association between EPHX1 (Tyr113His and His139Arg) polymorphisms and esophageal cancer risk by meta-analysis. | 24615030 | 2014 | ||||
|
0.080 | GeneticVariation | disease | BEFREE | This meta-analysis suggests that the p.Tyr113His and p.His139Arg polymorphisms in EPHX1 may not be associated with EC development. | 24803829 | 2014 | ||||
|
0.080 | GeneticVariation | disease | BEFREE | We investigated the association of EPHX1 Tyr113His and His139Arg polymorphisms with esophageal cancer via a comprehensive meta-analysis. | 24222229 | 2013 | ||||
|
0.080 | GeneticVariation | disease | BEFREE | Meta-analysis of these seven studies for EPHX1 His139Arg polymorphism showed that EPHX1 His139Arg polymorphism was also not associated with esophageal cancer risk under all genetic models. | 23681797 | 2013 | ||||
|
0.080 | GeneticVariation | disease | BEFREE | This case-control study investigated whether these polymorphisms in the EPHX1 gene influence esophageal cancer susceptibility in a Dutch Caucasian population. | 22447130 | 2012 | ||||
|
0.080 | GeneticVariation | disease | BEFREE | The present case-control study evaluated the influence of EPHX1 genetic variations on esophageal cancer susceptibility in 142 patients and 185 healthy controls from a high-incidence region of India where tobacco use and alcohol consumption are widespread and the users of these two substances are also betel quid chewers. | 20659238 | 2010 | ||||
|
0.080 | GeneticVariation | disease | BEFREE | The present results suggest that CYP1A1 3' polymorphism may be one of the promising protective factors and its wild gene type may be an indicator for higher susceptibility to esophageal cancer. mEH slow allele variant, associated with the progression of esophageal precancerous lesions, may contribute to the high susceptibility to esophageal carcinoma. | 12854128 | 2003 |