Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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: 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: 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: 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: rs10972727
rs10972727
0.010 GeneticVariation BEFREE We found that the G allele of rs11788747 in the RECK gene was significantly associated with WT in Chinese children (OR=0.7, 95% CI: 0.45-0.99; P=0.042); as with another SNP rs10972727, however, no statistically significant difference was detected. 26141647

2015

dbSNP: rs110419
rs110419
0.010 GeneticVariation BEFREE Only rs110419 AG was found to be protective against Wilms' tumor (adjusted OR = 0.62, 95% CI = 0.41-0.94, <i>P</i> = 0.024) when compared to rs110419 AA. 28881592

2017

dbSNP: rs1131691014
rs1131691014
0.010 GeneticVariation BEFREE Overall, our result suggested a lack of association between the <i>TP53</i> gene Arg72Pro polymorphism and Wilms' tumor. 28260929

2017

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: rs11788747
rs11788747
0.010 GeneticVariation BEFREE The present data indicate that there is a significant association between mutant G of rs11788747 in RECK and WT risk. 26141647

2015

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: rs1217691063
rs1217691063
0.010 GeneticVariation BEFREE Impact of the MTHFR C677T polymorphism on risk of Wilms tumor: case-control study. 19346876

2009

dbSNP: rs121912657
rs121912657
0.010 GeneticVariation BEFREE We show that (i) in the choroid plexus carcinoma, the germline mutation was detected in a homozygous state due to copy-neutral LOH/uniparental disomy, (ii) in the secondary AML, a complex karyotype led to loss of the wild-type TP53 allele, (iii) in the Wilms tumor, the somatic mutation c.814G>A led to compound heterozygosity. 25787918

2015

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: rs121913409
rs121913409
0.010 GeneticVariation BEFREE Three mutations, Ser45Phe (TCT --> TTT), Ser45Tyr (TCT --> TAT), and Delta45 (deletion of TCT), were found in 3 of 19 unilateral WTs. 12239584

2002

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: rs1423753702
rs1423753702
WT1
0.010 GeneticVariation BEFREE We report on a novel WT1 nonsense mutation (c.1105C>T), introducing a premature stop codon in exon 8 (p.Q369X), in a young XY male patient who presented with bilateral cryptorchidism, nystagmus, mild proteinuria and WT, but no sign of severe nephropathy. 19048299

2009

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: 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: rs2857461
rs2857461
0.010 GeneticVariation BEFREE One SNP in EWSR1 (rs2857461) showed a low level of statistical association with the diagnosis of Ewing sarcoma compared to Wilms tumor. 21793187

2012

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