Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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 The assay allows evaluating WT1 rs16754 polymorphism in diagnostic routine to improve prognostic information faster and without over-costing for diagnostic laboratories. 29407184

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 single-nucleotide polymorphism (SNP) within Wilms tumor-1 (WT1) exon 7, rs16754, has been arguably reported to be implicated in acute myeloid leukemia (AML) prognosis. 26499507

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 Wilms tumor gene single nucleotide polymorphism rs16754 predicts a favorable outcome in children with acute lymphoblastic leukemia. 26224397

2015

dbSNP: rs16754
rs16754
WT1
0.100 GeneticVariation BEFREE The Wilms' tumour gene 1 (WT1) single nucleotide polymorphism (SNP) rs16754 has recently been described as an independent prognostic factor in acute myeloid leukaemia (AML) patients. 23484026

2013

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

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 Clinical outcome and gene- and microRNA-expression profiling according to the Wilms tumor 1 (WT1) single nucleotide polymorphism rs16754 in adult de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study. 21659357

2011