Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131691014
rs1131691014
0.070 GeneticVariation BEFREE Thus, it is evident from our study that Arg72Pro SNP is implicated in bladder cancer, and that the rare, proline-related allele is connected with higher susceptibility to bladder cancer. 21156242

2010

dbSNP: rs1131691014
rs1131691014
0.070 GeneticVariation BEFREE P53 Arg72Pro polymorphism and bladder cancer risk--meta-analysis evidence for a link in Asians but not Caucasians. 22901221

2012

dbSNP: rs1131691014
rs1131691014
0.070 GeneticVariation BEFREE Subgroup analyses by ethnicity showed that TP53 Arg72Pro polymorphism contributed to bladder cancer</span> risk in East Asians in three genetic models (For Pro vs. Arg, Fixed-effects OR 1.18, 95 % CI 1.05-1.32; For ProPro vs. ArgArg, Fixed-effects OR 1.40, 95 % CI 1.11-1.77; For ProPro vs. ArgPro/ArgArg, Fixed-effects OR 1.32, 95 % CI 1.07-1.62). 23184052

2013

dbSNP: rs1131691014
rs1131691014
0.070 GeneticVariation BEFREE This meta-analysis suggests that p53 Arg72Pro polymorphism is associated with increased risk of bladder cancer in Asians. 23073555

2013

dbSNP: rs1131691014
rs1131691014
0.070 GeneticVariation BEFREE Meta-analysis of association between TP53 Arg72Pro polymorphism and bladder cancer risk. 20630574

2010

dbSNP: rs1131691014
rs1131691014
0.070 GeneticVariation BEFREE The role of TP53 PRO47SER and ARG72PRO single nucleotide polymorphisms in the susceptibility to bladder cancer. 19523860

2011

dbSNP: rs113488022
rs113488022
0.010 GeneticVariation BEFREE Homologous Mutation to Human BRAF V600E Is Common in Naturally Occurring Canine Bladder Cancer--Evidence for a Relevant Model System and Urine-Based Diagnostic Test. 25767210

2015

dbSNP: rs1135612
rs1135612
POR
0.010 GeneticVariation BEFREE In this study, we first sequenced all 16 POR exons among 50 randomly selected controls, and found three variants, rs1135612, rs1057868 (A503V) and rs2228104, which were then assessed the relation to risk of bladder cancer in a case-control study of 1,050 bladder cancer cases and 1,404 cancer-free controls in a Chinese population. 26123203

2015

dbSNP: rs1136410
rs1136410
0.010 GeneticVariation BEFREE Using multifactor dimensionality reduction approach, the four-factor model, including smoking status, OGG1 S326C (rs1052133), APEX1 D148E (rs3136820), and ADPRT762 (rs1136410), had the best ability to predict bladder cancer risk with the highest cross-validation consistency (100%) and the lowest prediction error (37.02%; P < 0.001). 17220334

2007

dbSNP: rs1141718
rs1141718
0.010 GeneticVariation BEFREE The detoxifying enzymes inactivate dangerous chemical compounds and anions for the cell; that is, why it is important to know if the polymorphisms pro198leu in GPX-1 and ile58thr in MnSOD are associated with bladder cancer. 20441054

2010

dbSNP: rs11466445
rs11466445
0.010 GeneticVariation BEFREE The distribution of the TGFBR1*6A allele (rs11466445) was also similar among cases and controls, indicating no association with bladder cancer risk. 19004027

2009

dbSNP: rs11543198
rs11543198
0.010 GeneticVariation BEFREE SNP rs8041357, which is in complete linkage disequilibrium (r(2) = 1) with rs11543198, was also associated with bladder cancer risk in Europeans (P = 0.045 for an additive and P = 0.025 for a recessive model), despite much lower minor allele frequency in Europeans (3.7%) compared with the Japanese (22.2%). 25281661

2015

dbSNP: rs11614913
rs11614913
0.040 GeneticVariation BEFREE We found that CT (miR-196a2, C>T rs11614913) was a risk factor for renal cell carcinoma (CT vs. CC: OR = 1.72, 95%CI = 1.05-2.80, <i>P</i> = 0.03, <i>I</i><sup>2</sup> = 66%), especially in Asian population (CT vs. CC: OR = 1.17, 95%CI = 1.04-1.32, <i>P</i> < 0.01, <i>I</i><sup>2</sup> = 0%). miR-146a G>C rs2910164 was a protective factor of urological cancers (C vs. G: OR = 0.87, 95%CI = 0.81-0.93, <i>P</i> < 0.01, <i>I</i><sup>2</sup> = 0%), especially for bladder cancer. miR-499 A>G rs3746444 was correlated with an increased risk of urological cancers, specifically in Asian population. 28579964

2017

dbSNP: rs11614913
rs11614913
0.040 GeneticVariation BEFREE Even though there was no association between the individuals carrying the variant genotypes of the three miRNA studied and bladder cancer risk, marginal significance of heterozygousity in rs11614913 suggested further characterization of miRNA SNPs in a large cohort of varied ethnicity. 21345130

2011

dbSNP: rs11614913
rs11614913
0.040 GeneticVariation BEFREE Our results suggested hsa-mir-196a2 rs11614913 C/T is associated with a significantly decreased risk of bladder cancer and hsa-mir-146a rs2910164 GG genotype is associated with clinical stage and metastasis in bladder cancer. 26458899

2015

dbSNP: rs11614913
rs11614913
0.040 GeneticVariation BEFREE Further, rs11614913 was found to be significantly associated with decreased cancer risk, in particular, for bladder cancer, gastric cancer, and SCCHN. 24278149

2013

dbSNP: rs11671784
rs11671784
0.010 GeneticVariation BEFREE This study identified a causative relationship between rs11671784 G/A variation, lowered miR-27a expression, increased RUNX-1 expression and following weakened chemo-sensitivity. rs11671784 G allele has significantly stronger effect over A allele in promoting chemo-sensitivity in bladder cancer. miR-27a mediates chemotherapy at least partially through reducing P-gp expression and increasing apoptosis. 25656571

2015

dbSNP: rs11685387
rs11685387
0.010 GeneticVariation BEFREE In this hospital-based case-control study, the association of Ku80 G-1401T rs828907, Ku80 C-319T rs11685387 and Ku80 intron 19 rs9288518 polymorphisms with bladder cancer risk in a central Taiwanese population was investigated. 19414375

2009

dbSNP: rs11871756
rs11871756
0.010 GeneticVariation BEFREE Four variants within ZIP11 were significantly associated with bladder cancer risk: rs11871756 (OR = 1.43, 95 % CI (1.24-1.63), p = 0.0002), rs11077654 (OR = 0.76, 95 % CI (0.68-0.85), p = 0.001), rs9913017 (OR = 0.76, 95 % CI (0.68-0.85), p = 0.002), and rs4969054 (OR = 0.78, 95 % CI (0.69-0.88), p = 0.02); the three protective variants were co-located and highly correlated. 25900876

2015

dbSNP: rs11892031
rs11892031
0.730 GeneticVariation BEFREE Using data on high-risk occupations for 2258 case patients and 2410 control patients from two bladder cancer studies, we observed that three of 16 known or candidate bladder cancer susceptibility variants displayed statistically significant and consistent evidence of additive interactions; specifically, the GSTM1 deletion polymorphism (P interaction ≤ .001), rs11892031 (UGT1A, P interaction = .01), and rs798766 (TMEM129-TACC3-FGFR3, P interaction = .03). 26374428

2015

dbSNP: rs11892031
rs11892031
0.730 GeneticVariation GWASDB In a combined analysis, we identified three new regions associated with bladder cancer on chromosomes 22q13.1, 19q12 and 2q37.1: rs1014971, (P = 8 × 10⁻¹²) maps to a non-genic region of chromosome 22q13.1, rs8102137 (P = 2 × 10⁻¹¹) on 19q12 maps to CCNE1 and rs11892031 (P = 1 × 10⁻⁷) maps to the UGT1A cluster on 2q37.1. 20972438

2010

dbSNP: rs11892031
rs11892031
0.730 GeneticVariation BEFREE In a combined analysis, we identified three new regions associated with bladder cancer on chromosomes 22q13.1, 19q12 and 2q37.1: rs1014971, (P = 8 × 10⁻¹²) maps to a non-genic region of chromosome 22q13.1, rs8102137 (P = 2 × 10⁻¹¹) on 19q12 maps to CCNE1 and rs11892031 (P = 1 × 10⁻⁷) maps to the UGT1A cluster on 2q37.1. 20972438

2010

dbSNP: rs11892031
rs11892031
0.730 GeneticVariation BEFREE Results showed that heterogeneity in ORs of tumor categories was not significant for either rs11892031 or rs401681 (p>0.05), indicating that the two SNPs seemingly do not associate with tumor grade and stage of bladder cancer in our study population. 25347272

2014

dbSNP: rs11892031
rs11892031
A 0.730 GeneticVariation GWASDB Genome-wide association study identifies multiple loci associated with bladder cancer risk. 24163127

2014

dbSNP: rs1189516787
rs1189516787
0.010 GeneticVariation BEFREE The luciferase assays further showed that there was a point mutation (A231G) in the C/EBPα binding site of the lncRNA-UCA1 core promoter in various bladder cancer cell lines, which in turn significantly increased the transcriptional activity of lncRNA-UCA1. 24648007

2014