Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12921862
rs12921862
0.010 GeneticVariation BEFREE The <i>AXIN1</i> gene polymorphisms might implicate in BC risk, and rs12921862 could be a potential forecasting factor for prognosis of BC patients. 31143301

2019

dbSNP: rs138377917
rs138377917
0.010 GeneticVariation BEFREE Cumulative evidence of an association was graded as strong for rs2294008 [odds ratio (OR) = 1.32, P = 5.1 × 10-33], rs2976392 (OR = 1.29, P = 1.8 × 10-8), rs9297976 (OR = 0.75, P = 1.4 × 10-7), rs2976391 (OR = 1.38, P = 6.1 × 10-5) and rs138377917 (OR = 0.53, P = 0.008) with gastric cancer, rs2294008 with bladder cancer (OR = 1.15, P = 8.0 × 10-19), gastritis (OR = 1.35, P = 1.2 × 10-5), duodenal ulcer (OR = 0.68, P = 2.4 × 10-57) and gastric ulcer (OR = 0.88, P = 1.7 × 10-7). 30407486

2019

dbSNP: rs1805105
rs1805105
0.010 GeneticVariation BEFREE Our data revealed that three tag SNPs were associated with an increased risk of BC (rs12921862: <i>P</i> < 0.001, OR (95%CI) = 4.61 (3.13-6.81); rs1805105: <i>P</i> = 0.046, OR (95%CI) = 1.35 (1.00-1.82); and rs370681: <i>P</i> = 0.004, OR (95%CI) = 1.56 (1.15-2.10)). 31143301

2019

dbSNP: rs2067079
rs2067079
0.010 GeneticVariation BEFREE The T G haplotype (rs2067079 and rs6790) increased the risk of bladder cancer in the assessed population (OR (95% CI) = 1.73 (1.18-2.56), adjusted P value = 0.02). 31250374

2019

dbSNP: rs2073859
rs2073859
0.010 GeneticVariation BEFREE PCR-Restriction Fragment Length Polymorphism (RFLP) was used to genotype LIMK2 SNP rs2073859 and multivariate logistic regression applied to assess the relationship between allele frequency and clinical features in 139 BC patients. 30006972

2019

dbSNP: rs2278329
rs2278329
0.010 GeneticVariation BEFREE Patients with bladder cancer and controls did not differ significantly in terms of genotype frequencies and allele frequency distribution of rs2278329 (P = 0.77, OR = 0.97) and rs2292016 (P = 0.39, OR = 1.20) respectively. 30755233

2019

dbSNP: rs2292016
rs2292016
0.010 GeneticVariation BEFREE Patients with bladder cancer and controls did not differ significantly in terms of genotype frequencies and allele frequency distribution of rs2278329 (P = 0.77, OR = 0.97) and rs2292016 (P = 0.39, OR = 1.20) respectively. 30755233

2019

dbSNP: rs2293607
rs2293607
0.010 GeneticVariation BEFREE At the end of the study, we suggested that there may exist an association between a combination of MYNN rs10936599 and TERC rs2293607 polymorphisms and development of bladder cancer in Turkish population. 30120764

2019

dbSNP: rs2735971
rs2735971
0.010 GeneticVariation BEFREE Association between lncRNA H19 (rs217727, rs2735971 and rs3024270) polymorphisms and the risk of bladder cancer in Chinese population. 29595036

2019

dbSNP: rs2976391
rs2976391
PSCA ; JRK
0.010 GeneticVariation BEFREE Cumulative evidence of an association was graded as strong for rs2294008 [odds ratio (OR) = 1.32, P = 5.1 × 10-33], rs2976392 (OR = 1.29, P = 1.8 × 10-8), rs9297976 (OR = 0.75, P = 1.4 × 10-7), rs2976391 (OR = 1.38, P = 6.1 × 10-5) and rs138377917 (OR = 0.53, P = 0.008) with gastric cancer, rs2294008 with bladder cancer (OR = 1.15, P = 8.0 × 10-19), gastritis (OR = 1.35, P = 1.2 × 10-5), duodenal ulcer (OR = 0.68, P = 2.4 × 10-57) and gastric ulcer (OR = 0.88, P = 1.7 × 10-7). 30407486

2019

dbSNP: rs2976392
rs2976392
PSCA ; JRK
0.010 GeneticVariation BEFREE Cumulative evidence of an association was graded as strong for rs2294008 [odds ratio (OR) = 1.32, P = 5.1 × 10-33], rs2976392 (OR = 1.29, P = 1.8 × 10-8), rs9297976 (OR = 0.75, P = 1.4 × 10-7), rs2976391 (OR = 1.38, P = 6.1 × 10-5) and rs138377917 (OR = 0.53, P = 0.008) with gastric cancer, rs2294008 with bladder cancer (OR = 1.15, P = 8.0 × 10-19), gastritis (OR = 1.35, P = 1.2 × 10-5), duodenal ulcer (OR = 0.68, P = 2.4 × 10-57) and gastric ulcer (OR = 0.88, P = 1.7 × 10-7). 30407486

2019

dbSNP: rs3024270
rs3024270
0.010 GeneticVariation BEFREE Association between lncRNA H19 (rs217727, rs2735971 and rs3024270) polymorphisms and the risk of bladder cancer in Chinese population. 29595036

2019

dbSNP: rs370681
rs370681
0.010 GeneticVariation BEFREE Our data revealed that three tag SNPs were associated with an increased risk of BC (rs12921862: <i>P</i> < 0.001, OR (95%CI) = 4.61 (3.13-6.81); rs1805105: <i>P</i> = 0.046, OR (95%CI) = 1.35 (1.00-1.82); and rs370681: <i>P</i> = 0.004, OR (95%CI) = 1.56 (1.15-2.10)). 31143301

2019

dbSNP: rs4143815
rs4143815
0.010 GeneticVariation BEFREE Subgroup analysis based on cancer type suggested that PD-L1 rs4143815 C > G might increase the susceptibility to gastric cancer (G vs. C: OR = 1.842, 95% CI: 1.403-2.418, p < 0.001) and bladder cancer (G vs. C: OR = 2.015, 95% CI: 1.556-2.608, p < 0.001), and genotype GG carriers of PD-L1 rs4143815 C > G might have higher risks of HCC (GG vs. CG + CC: OR = 2.226 95% CI: 1.562-3.172, p < 0.001). 30552042

2019

dbSNP: rs6790
rs6790
0.010 GeneticVariation BEFREE The T G haplotype (rs2067079 and rs6790) increased the risk of bladder cancer in the assessed population (OR (95% CI) = 1.73 (1.18-2.56), adjusted P value = 0.02). 31250374

2019

dbSNP: rs8444
rs8444
0.010 GeneticVariation BEFREE Our results showed that LASS2-3'-UTR r</span>s8444 C>T polymorphism was significantly associated with the individual risk and the poor overall survival of bladder cancer, suggesting that rs8444 TT genotype maybe act as an independent risk factor of susceptibility and clinical prognosis for bladder cancer in Chinese population. 31577563

2019

dbSNP: rs9297976
rs9297976
PSCA ; JRK
0.010 GeneticVariation BEFREE Cumulative evidence of an association was graded as strong for rs2294008 [odds ratio (OR) = 1.32, P = 5.1 × 10-33], rs2976392 (OR = 1.29, P = 1.8 × 10-8), rs9297976 (OR = 0.75, P = 1.4 × 10-7), rs2976391 (OR = 1.38, P = 6.1 × 10-5) and rs138377917 (OR = 0.53, P = 0.008) with gastric cancer, rs2294008 with bladder cancer (OR = 1.15, P = 8.0 × 10-19), gastritis (OR = 1.35, P = 1.2 × 10-5), duodenal ulcer (OR = 0.68, P = 2.4 × 10-57) and gastric ulcer (OR = 0.88, P = 1.7 × 10-7). 30407486

2019

dbSNP: rs11191438
rs11191438
0.010 GeneticVariation BEFREE AS3MT rs11191438 (C > G) G/G genotype, AS3MT rs10748835 (A > G) G/G genotype, and AS3MT rs1046778 (C > T) T/T genotype were found to be related to BC risk, where the odds ratio (OR) (95% CI) was 0.50 (0.31-0.82), 0.49 (0.30-0.79), and 0.54 (0.36-0.80), respectively. 29669044

2018

dbSNP: rs11191454
rs11191454
0.010 GeneticVariation BEFREE The polymorphisms of AS3MT rs11191438, AS3MT rs10748835, and AS3MT rs1046778 were related to the risk of BC and UTUC, while the polymorphisms of AS3MT rs3740393, AS3MT rs11191453, and AS3MT rs11191454 were associated with arsenic methylation capacity. 29859237

2018

dbSNP: rs1130214
rs1130214
0.010 GeneticVariation BEFREE None of the other examined polymorphisms (<i>AKT1</i> rs1130214, <i>AKT1</i> rs3730358, <i>mTOR</i> rs1883965) revealed significant association with BC. 29383014

2018

dbSNP: rs1130233
rs1130233
0.010 GeneticVariation BEFREE In conclusion, our findings suggest that <i>PIK3CA</i> rs6443624, <i>AKT1</i> rs2498801, <i>AKT1</i> rs1130233, as well <i>mTOR</i> rs2295080 polymorphism may be related to bladder cancer development in a sample of Iranian population. 29383014

2018

dbSNP: rs13278062
rs13278062
0.010 GeneticVariation BEFREE The single nucleotide polymorphism (SNP), -397G > T (rs13278062) polymorphism, in the promoter of Death Receptor 4 (DR4) had been reported to be associated with a significantly increased risk for bladder cancer. 29446085

2018

dbSNP: rs1428779969
rs1428779969
PXN
0.010 GeneticVariation BEFREE LPXN may facilitate bladder cancer progression by upregulating the expression of S100P via PI3K/AKT pathway. 29975926

2018

dbSNP: rs1883965
rs1883965
0.010 GeneticVariation BEFREE None of the other examined polymorphisms (<i>AKT1</i> rs1130214, <i>AKT1</i> rs3730358, <i>mTOR</i> rs1883965) revealed significant association with BC. 29383014

2018

dbSNP: rs2295080
rs2295080
0.010 GeneticVariation BEFREE Additionally, mTOR rs2295080 variant notably increased the risk of BC (OR=2.25, 95 % CI=1.50-3.38, p<0.0001, GT vs GG; OR=4.75, 95 % CI=2.80-8.06, p<0.0001, TT vs GG; OR=3.10, 95 % CI=2.34-4.10, p<0.0001, T vs G). 29383014

2018