Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1042522
rs1042522
0.020 GeneticVariation BEFREE The effect of rs1042522 C>G polymorphism on Wilms tumor prevalence was analyzed using logistic regression models. 30610160

2019

dbSNP: rs11655237
rs11655237
0.020 GeneticVariation BEFREE These data could be useful for reinforcing our understanding of the potential contribution of LINC00673 rs11655237 C>T to Wilms tumor susceptibility. 31657076

2019

dbSNP: rs11655237
rs11655237
0.020 GeneticVariation BEFREE In conclusion, we failed to find any association between the LINC00673 rs11655237 C>T polymorphism and WT risk. 31257678

2019

dbSNP: rs1042522
rs1042522
0.020 GeneticVariation BEFREE Overall, our result suggested a lack of association between the <i>TP53</i> gene Arg72Pro polymorphism and Wilms' tumor. 28260929

2017

dbSNP: rs16754
rs16754
WT1
0.020 GeneticVariation BEFREE Wilms tumor gene single nucleotide polymorphism rs16754 predicts a favorable outcome in children with acute lymphoblastic leukemia. 26224397

2015

dbSNP: rs16754
rs16754
WT1
0.020 GeneticVariation BEFREE The genetic variant rs16754 of Wilms tumor gene 1 (WT1) has recently been described as an independent prognostic factor in AML patients. 25932444

2015

dbSNP: rs376882637
rs376882637
0.010 GeneticVariation BEFREE Our findings suggest that TRIP13 c.1060C>T mutation may be infrequent in Pakistani WT cases. 31574018

2020

dbSNP: rs1059111
rs1059111
0.010 GeneticVariation BEFREE The association between rs11994014 G>A or rs1059111 A>T polymorphisms and Wilms' tumor susceptibility did not reach statistical significance. 31057612

2019

dbSNP: rs113488022
rs113488022
0.010 GeneticVariation BEFREE In summary, we demonstrate that BRA</span>F V600E mutations are not entirely restricted to typical MA, as they may be seen in MAs showing mitotic activity along with a subset of epithelial-predominant WTs in adults and children that have foci which overlap morphologically with MA. 31192863

2019

dbSNP: rs11994014
rs11994014
0.010 GeneticVariation BEFREE The association between rs11994014 G>A or rs1059111 A>T polymorphisms and Wilms' tumor susceptibility did not reach statistical significance. 31057612

2019

dbSNP: rs121913377
rs121913377
0.010 GeneticVariation BEFREE In summary, we demonstrate that BRA</span>F V600E mutations are not entirely restricted to typical MA, as they may be seen in MAs showing mitotic activity along with a subset of epithelial-predominant WTs in adults and children that have foci which overlap morphologically with MA. 31192863

2019

dbSNP: rs12587
rs12587
0.010 GeneticVariation BEFREE Stratification analysis revealed that rs12587 GT/TT was associated with Wilms tumor risk in children >18 months old (adjusted OR=1.39, 95% CI=1.02-1.89, <i>P</i>=0.037). 30860980

2019

dbSNP: rs2168101
rs2168101
0.010 GeneticVariation BEFREE These results suggest that <i>LMO1</i> gene rs2168101 G>T polymorphism may help prevent Wilms tumor, but this conclusion should be verified in other populations and additional studies. 31205537

2019

dbSNP: rs28647582
rs28647582
0.010 GeneticVariation BEFREE Our study suggested that PHOX2B rs28647582 T>C was weakly associated with Wilms tumor susceptibility. 31652452

2019

dbSNP: rs2979704
rs2979704
0.010 GeneticVariation BEFREE Our findings suggested that the <i>NEFL</i> rs2979704 T>C polymorphism may be associated with Wilms' tumor susceptibility in the Chinese population. 31057612

2019

dbSNP: rs57961569
rs57961569
0.010 GeneticVariation BEFREE Interestingly, in the stratification analysis, the rs57961569 was found to be associated with decreased Wilms tumor susceptibility in the children older than 18 months (AOR = 0.65, 95% CI = 0.42-1.00, P = .050). 31343784

2019

dbSNP: rs6581658
rs6581658
0.010 GeneticVariation BEFREE We carried out the first four-center case-control study with 355 patients and 1070 controls to assess the association of HMGA2 polymorphisms (rs6581658 A>G, rs8756 A>C, and rs968697 T>C) with Wilms tumor risk. 31746066

2019

dbSNP: rs8173
rs8173
0.010 GeneticVariation BEFREE In conclusion, our findings indicated that the <i>AURKA</i> rs8173 G>C polymorphism was associated with decreased Wilms tumor risk in Chinese children. 31636670

2019

dbSNP: rs8756
rs8756
0.010 GeneticVariation BEFREE We carried out the first four-center case-control study with 355 patients and 1070 controls to assess the association of HMGA2 polymorphisms (rs6581658 A>G, rs8756 A>C, and rs968697 T>C) with Wilms tumor risk. 31746066

2019

dbSNP: rs968697
rs968697
0.010 GeneticVariation BEFREE We firstly demonstrated that rs6581658 A>G, rs8756 A>C, and rs968697 T>C could not impact Wilms tumor risk, respectively. 31746066

2019

dbSNP: rs1052133
rs1052133
0.010 GeneticVariation BEFREE Significant associations with Wilms tumor susceptibility were shown for hOGG1 rs1052133 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.96, P = .030), FEN1 rs174538 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.95, P = .027; recessive: adjusted OR = 0.54, 95% CI = 0.32-0.93 P = .027), and FEN1 rs4246215 (dominant: adjusted OR = 0.55, 95% CI = 0.38-0.80, P = .002) polymorphisms. 29937070

2018

dbSNP: rs174538
rs174538
0.010 GeneticVariation BEFREE Significant associations with Wilms tumor susceptibility were shown for hOGG1 rs1052133 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.96, P = .030), FEN1 rs174538 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.95, P = .027; recessive: adjusted OR = 0.54, 95% CI = 0.32-0.93 P = .027), and FEN1 rs4246215 (dominant: adjusted OR = 0.55, 95% CI = 0.38-0.80, P = .002) polymorphisms. 29937070

2018

dbSNP: rs314276
rs314276
0.010 GeneticVariation BEFREE In summary, these results indicated that the LIN28B gene rs314276 C>A polymorphism alone and three combined polymorphisms may be able to modify WT susceptibility in Southern Chinese children. 28301057

2018

dbSNP: rs3810366
rs3810366
0.010 GeneticVariation BEFREE The XPD rs3810366 polymorphism significantly enhanced Wilms tumor risk (dominant model: adjusted OR = 2.12, 95% CI = 1.26-3.57). 30161024

2018

dbSNP: rs4246215
rs4246215
0.010 GeneticVariation BEFREE Significant associations with Wilms tumor susceptibility were shown for hOGG1 rs1052133 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.96, P = .030), FEN1 rs174538 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.95, P = .027; recessive: adjusted OR = 0.54, 95% CI = 0.32-0.93 P = .027), and FEN1 rs4246215 (dominant: adjusted OR = 0.55, 95% CI = 0.38-0.80, P = .002) polymorphisms. 29937070

2018