Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs20417
rs20417
0.040 GeneticVariation BEFREE The aim of this study was to investigate the association between the cyclooxygenase 2 (COX2) -765G>C (rs20417) polymorphism and prostate cancer (PC) risk using meta-analysis. 26535654

2015

dbSNP: rs20417
rs20417
0.040 GeneticVariation BEFREE When all groups were pooled, we did not detect a significant association of rs20417 polymorphism with prostate cancer risk. 22782583

2012

dbSNP: rs20417
rs20417
0.040 GeneticVariation BEFREE In a hospital-based case/control study, 195 subjects with PCa and 250 healthy controls were investigated for the association of COX-2 -765 G>C (rs20417) and +8473 T>C (rs5275) promoter polymorphism with PCa susceptibility using the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method. 22023987

2011

dbSNP: rs20417
rs20417
0.040 GeneticVariation BEFREE We found no evidence that rs20417</span> alters prostate cancer</span> risk (odds</span> ratio (OR(CC & GC v GG)=1.05, 95% confidence interval (CI)=0.91-1.20). 19488068

2009

dbSNP: rs2745557
rs2745557
0.030 GeneticVariation BEFREE Also, the coexistence of COX-2 (rs2745557) and obesity, smoking, or diabetes may lead to the development of PCa or BPH. 26920155

2016

dbSNP: rs2745557
rs2745557
0.030 GeneticVariation BEFREE Based on our meta-analysis, COX-2 rs2745557 was associated with a lower PCa risk under dominant model in Caucasians. 22435969

2012

dbSNP: rs2745557
rs2745557
0.030 GeneticVariation BEFREE Three SNPs demonstrated nominally statistically significant associations with prostate cancer risk, with the most compelling polymorphism (rs2745557) associated with a lower risk of disease (odds ratio (OR) GC vs GG=0.64; 95% confidence interval (CI): 0.49-0.84; P=0.002). 17609663

2007

dbSNP: rs5275
rs5275
0.020 GeneticVariation BEFREE In a hospital-based case/control study, 195 subjects with PCa and 250 healthy controls were investigated for the association of COX-2 -765 G>C (rs20417) and +8473 T>C (rs5275) promoter polymorphism with PCa susceptibility using the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method. 22023987

2011

dbSNP: rs5275
rs5275
0.020 GeneticVariation BEFREE In PLCO, the Ex10 +837 T>C marker (rs5275) was initially associated with prostate cancer risk (P-trend = 0.02) but became non-significant after adjustment for multiple comparisons (P = 0.08); this SNP showed no association with prostate cancer risk in the Nutrition Cohort (P-trend = 0.54) or in an analysis pooling the two cohorts (P-trend = 0.20). 17999989

2008

dbSNP: rs689465
rs689465
0.010 GeneticVariation BEFREE Our results support the hypothesis that rs689465 influences susceptibility to prostate cancer; however, prostate cancer progression was not associated with rs689465 in a Japanese population. 24203817

2014

dbSNP: rs748500299
rs748500299
0.010 GeneticVariation BEFREE This study demonstrated a relationship between the COX2 G1195A variant and prostate cancer risk. 24203817

2014

dbSNP: rs689470
rs689470
0.010 GeneticVariation BEFREE However, we found that rs689470</span> was significantly associated with a trend towards increased prosta</span>te cancer risk when using both additive (OR = 2.15, 95%CI = 1.04-4.44, P = 0.04) and recessive models (OR = 2.07, 95%CI = 1.07-4.03, P = 0.03) to analyze the data. 22782583

2012

dbSNP: rs689466
rs689466
0.010 GeneticVariation BEFREE After adjustment for confounders, polymorphisms in COX-2 (rs689466) and IL-8 (rs4073) were not significantly associated with prostate cancer risk. 20431935

2010