Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16754
rs16754
WT1
0.040 GeneticVariation BEFREE The single nucleotide polymorphism (SNP) rs16754 of the WT1 gene has been previously described as a possible prognostic marker in normal karyotype acute myeloid leukemia (AML) patients. 23070125

2012

dbSNP: rs16754
rs16754
WT1
0.040 GeneticVariation BEFREE In Korean patients with CN-AML, WT1 SNP rs16754 had no significant impact on clinical outcomes and further investigations are needed to define prognostic implication of WT1 SNP rs16754 in CN-AML. 22015946

2012

dbSNP: rs16754
rs16754
WT1
0.040 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

dbSNP: rs16754
rs16754
WT1
0.040 GeneticVariation BEFREE WT1 SNP rs16754 may be a novel independent favorable-risk marker in CN-AML patients that might improve risk and treatment stratification. 20038731

2010

dbSNP: rs1057520018
rs1057520018
0.010 GeneticVariation BEFREE Phe354Leu Polymorphism of <i>LKB1</i> Is a Potential Prognostic Factor for Cytogenetically Normal Acute Myeloid Leukemia. 28882949

2018

dbSNP: rs536880332
rs536880332
0.010 GeneticVariation BEFREE Phe354Leu Polymorphism of <i>LKB1</i> Is a Potential Prognostic Factor for Cytogenetically Normal Acute Myeloid Leukemia. 28882949

2018

dbSNP: rs59912467
rs59912467
0.010 GeneticVariation BEFREE Phe354Leu Polymorphism of <i>LKB1</i> Is a Potential Prognostic Factor for Cytogenetically Normal Acute Myeloid Leukemia. 28882949

2018

dbSNP: rs2234593
rs2234593
WT1
0.010 GeneticVariation BEFREE The Wilms Tumor-1 (WT1) rs2234593 variant is a prognostic factor in normal karyotype acute myeloid leukemia. 26499507

2016

dbSNP: rs200945282
rs200945282
KIT
0.010 GeneticVariation BEFREE Cytogenetically normal acute myeloid leukemia with a novel KIT mutation in exon 11 G565V developing a sole trisomy 13 at relapse: a clinical dilemma. 24968822

2015

dbSNP: rs1424098571
rs1424098571
0.010 GeneticVariation BEFREE We analyzed polymorphisms in genes encoding cytidine deaminase (CDA 79A>C rs2072671 and -451C>T rs532545), 5'-nucleotidase (cN-II 7A>G rs10883841), and deoxycytidine kinase (DCK 3'UTR 948T>C rs4643786) in 205 de novo NK-AML patients. 23873772

2013

dbSNP: rs4643786
rs4643786
DCK
0.010 GeneticVariation BEFREE We analyzed polymorphisms in genes encoding cytidine deaminase (CDA 79A>C rs2072671 and -451C>T rs532545), 5'-nucleotidase (cN-II 7A>G rs10883841), and deoxycytidine kinase (DCK 3'UTR 948T>C rs4643786) in 205 de novo NK-AML patients. 23873772

2013

dbSNP: rs11554137
rs11554137
0.010 GeneticVariation BEFREE IDH1 SNP rs11554137 but not IDH1 R132 mutations are associated with an inferior outcome in CN-AML. 20368538

2010