Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1423753702
rs1423753702
WT1
0.710 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: rs10060683
rs10060683 		0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs11913239
rs11913239
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs1243010179
rs1243010179
CTCF
0.700 GeneticVariation UNIPROT

dbSNP: rs16988855
rs16988855
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs2009857
rs2009857
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs2221269
rs2221269
LOC105379082
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs2234584
rs2234584
WT1
0.700 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249

2013
dbSNP: rs2234584
rs2234584
WT1
0.700 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965

2015
dbSNP: rs2234584
rs2234584
WT1
0.700 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360

2017
dbSNP: rs2234584
rs2234584
WT1
0.700 GeneticVariation UNIPROT Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. 15604628

2004
dbSNP: rs2267166
rs2267166
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs61344503
rs61344503
LOC105379082
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: rs7288385
rs7288385
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs7288627
rs7288627
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs7290898
rs7290898
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs778634417
rs778634417
TTN ; TTN-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs8141515
rs8141515
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs16754
rs16754
WT1
0.100 GeneticVariation BEFREE SNP in the WT1 gene (rs16754) was significantly associated with lower expression of WT1. 30082223

2018
dbSNP: rs16754
rs16754
WT1
0.100 GeneticVariation BEFREE In conclusion, WT1 rs16754 polymorphism is associated with better survival of AML. 26992216

2016
dbSNP: rs16754
rs16754
WT1
0.100 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: rs16754
rs16754
WT1
0.100 GeneticVariation BEFREE The high prevalence of WT1 SNP rs16754, and its correlation with improved outcome, identifies WT1 SNP rs16754 as a potentially important molecular marker of prognosis in pediatric AML. 21189390

2011
dbSNP: rs16754
rs16754
WT1
0.100 GeneticVariation BEFREE The frequency of WT1 mutation in the Southeast Asian AML was thus comparable to the figures reported from the West although the designated major allele for rs16754 polymorphism was different. 21798259

2011
dbSNP: rs16754
rs16754
WT1
0.100 GeneticVariation BEFREE At least one copy of the minor SNP rs16754 allele (WT1(AG) or WT1(GG)) was detected in 30 (29 %) patients. 22895555

2012