Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3755132
rs3755132 		G 0.800 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs3755132
rs3755132 		G 0.800 GeneticVariation GWASCAT A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs807624
rs807624 		A 0.800 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs807624
rs807624 		A 0.800 GeneticVariation GWASCAT A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs10060683
rs10060683 		0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs6887553
rs6887553 		0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
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: rs8173
rs8173
AURKA
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: rs7585356
rs7585356
BARD1
0.010 GeneticVariation BEFREE Stratified analysis revealed that in term of clinical stage, rs7585356 AA carriers were associated with increased risk of developing clinical stage I+II nephroblastoma. 28161399

2017
dbSNP: rs113488022
rs113488022
BRAF
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: rs121913377
rs121913377
BRAF
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: rs28897756
rs28897756
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507327
rs397507327
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507404
rs397507404
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397508045
rs397508045
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs41293497
rs41293497
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs41293511
rs41293511
BRCA2
C 0.700 CausalMutation CLINVAR

dbSNP: rs80358391
rs80358391
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358427
rs80358427
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358435
rs80358435
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358557
rs80358557
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358721
rs80358721
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs80358785
rs80358785
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs80358807
rs80358807
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358814
rs80358814
BRCA2
T 0.700 CausalMutation CLINVAR