|
rs10060683
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies susceptibility loci for Wilms tumor.
|
22544364 |
2012 |
|
rs1027643
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies susceptibility loci for Wilms tumor.
|
22544364 |
2012 |
|
rs1027643
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies susceptibility loci for Wilms tumor.
|
22544364 |
2012 |
|
rs1037084691
|
|
|
0.010 |
GeneticVariation |
BEFREE |
WT1(R458Q) overexpression significantly downregulated nephrin and synaptopodin expression, promoted apoptosis in HEK293 cells and impaired focal contact formation in podocytes.
|
25145932 |
2015 |
|
rs1042522
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The effect of rs1042522 C>G polymorphism on Wilms tumor prevalence was analyzed using logistic regression models.
|
30610160 |
2019 |
|
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 |
|
rs104894855
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1049509674
|
|
|
0.010 |
GeneticVariation |
BEFREE |
analysis of the Wilms' tumour suppressor gene in a patient with Frasier syndrome by the polymerase chain reaction and direct sequencing detected a + 5G -->A transition at a position of the second alternative splice region of exon 9, important for predicting the risk of the occurrence of Wilms' tumour.
|
11954756 |
2002 |
|
rs1051266
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 rs1051266 (G80A) genotypes with the risk of developing nephroblastoma and neuroblastoma.
|
25536437 |
2015 |
|
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 |
|
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 |
|
rs1060501253
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs10767935
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Two-independent intronic genotyped SNPs (rs10767935 and rs5030244) in WT1 significantly modified the IFN-β-25(OH)D association after adjustment (P(interaction) = 0.001, 0.0002; P(adj) = 0.003, 0.006, respectively).
|
25312909 |
2015 |
|
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 |
|
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 |
|
rs1131690795
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
rs1188182005
|
|
|
0.010 |
GeneticVariation |
BEFREE |
analysis of the Wilms' tumour suppressor gene in a patient with Frasier syndrome by the polymerase chain reaction and direct sequencing detected a + 5G -->A transition at a position of the second alternative splice region of exon 9, important for predicting the risk of the occurrence of Wilms' tumour.
|
11954756 |
2002 |
|
rs11913239
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies susceptibility loci for Wilms tumor.
|
22544364 |
2012 |
|
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 |
|
rs1217691063
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 rs1051266 (G80A) genotypes with the risk of developing nephroblastoma and neuroblastoma.
|
25536437 |
2015 |