Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.040 GeneticVariation BEFREE MTHFR gene polymorphisms, the c. 677C>T and c. 1298A>C have been implicated as risk factors for several types of cancers as the acute leukemia. 28374953

2018

dbSNP: rs1217691063
rs1217691063
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.040 GeneticVariation BEFREE This study tested the hypothesis that maternal folic acid supplementation before or during pregnancy reduces AL risk, accounting for the SNPs rs1801133 (C677T) and rs1801131 (A1298C) in MTHFR and rs1801394 (A66G) and rs1532268 (C524T) in MTRR, assumed to modify folate metabolism. 22706675

2012

dbSNP: rs1217691063
rs1217691063
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.040 GeneticVariation BEFREE The MTHFR C677T and A1298C polymorphisms are not significant risk factors in adult acute leukemia in the Korean population. 17970089

2007

dbSNP: rs1217691063
rs1217691063
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.040 GeneticVariation BEFREE We retrospectively analyzed the incidence of MTHFR C677T and the influence of genotype on methotrexate (MTX) toxicity in patients with acute leukemia undergoing maintenance chemotherapy. 12453860

2002

dbSNP: rs1045642
rs1045642
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.030 GeneticVariation BEFREE Our results suggest that the ABCB1 G2677T and C3435T sequence variations may affect susceptibility to acute leukemia. 27706688

2016

dbSNP: rs1045642
rs1045642
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.030 GeneticVariation BEFREE ABCB1 3435C > T polymorphisms may be associated with susceptibility to acute leukemia, and ABCB1 polymorphisms might be a sensitive indicator for predicting efficacy of MTX therapy in the treatment of acute leukemia. 25921280

2015

dbSNP: rs1045642
rs1045642
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.030 GeneticVariation BEFREE Association of an MDR1 gene (C3435T) polymorphism with acute leukemia in India. 21133625

2010

dbSNP: rs77375493
rs77375493
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.030 GeneticVariation BEFREE A high JAK2(V617F) allele burden was correlated with the transformation to myelofibrosis (p<0.0001), but not with the transformation to acute leukemia. 22818858

2013

dbSNP: rs77375493
rs77375493
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.030 GeneticVariation BEFREE JAK2 V617F mutation was detected after transformation to CMML in 1 of them; in the other, a novel translocation t(5;12)(p13;q24) was observed at the time of progression to acute leukemia. 21658659

2011

dbSNP: rs77375493
rs77375493
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.030 GeneticVariation BEFREE JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia. 16037387

2005

dbSNP: rs397507444
rs397507444
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.020 GeneticVariation BEFREE This study tested the hypothesis that maternal folic acid supplementation before or during pregnancy reduces AL risk, accounting for the SNPs rs1801133 (C677T) and rs1801131 (A1298C) in MTHFR and rs1801394 (A66G) and rs1532268 (C524T) in MTRR, assumed to modify folate metabolism. 22706675

2012

dbSNP: rs397507444
rs397507444
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.020 GeneticVariation BEFREE The MTHFR C677T and A1298C polymorphisms are not significant risk factors in adult acute leukemia in the Korean population. 17970089

2007

dbSNP: rs1048943
rs1048943
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE The results of the present study suggest that CYP1A1 Ile462Val polymorphism might be a low-penetrant risk factor for acute leukemia. 23056546

2012

dbSNP: rs1057519766
rs1057519766
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE Three out of 14 (21.4 %) C57BL/6J mice transplanted with FLT3-N676K</span>-transduced primary hematopoietic progenitor cells developed acute leukemia (latency of 68, 77, and 273 days), while no hematological malignancy was observed in the control groups including FLT3-ITD. 26891877

2016

dbSNP: rs111033563
rs111033563
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE We studied the prevalence of 12 hereditary hemochromatosis (HH) gene mutations (C282Y, V53M, V59M, H63D, H63H, S56C, Q127H, E168Q, E168X, W169X and Q283P in the HFE gene and Y250X in the TFR2 gene) and its correlation with the iron status in 82 adult patients with acute leukemia (AL); 48 patients (58.5%) were affected by acute myeloid leukemia (AML) and 34 patients (41.5%) by acute lymphoblastic leukemia (ALL); 27 patients (32.9%) had at least one HH gene mutation (6 heterozygous for C282Y, 6 homozygous for H63D, 13 heterozygous for H63D and 2 heterozygous for S56C). 15863206

2005

dbSNP: rs1137101
rs1137101
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE The aim of the study was to evaluate bone marrow and peripheral blood leptin level and frequency of distribution of leptin receptor gene polymorphism Gln223Arg in children with acute leukemia. 17072067

2006

dbSNP: rs11978267
rs11978267
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE Two common polymorphisms in the IKZF1 gene (rs4132601 and rs11978267 variants) have been reported to be associated with childhood acute leukemia (AL) risk, however the results were inconsistent. 25423013

2014

dbSNP: rs121434592
rs121434592
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE This study demonstrated that the AKT1 E17K mutation occurs in breast cancers at a low frequency, and that it is rare in other common cancers, including colorectal, lung, gastric and hepatocellular carcinomas and acute leukaemias. 18392055

2008

dbSNP: rs121918464
rs121918464
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE Thus, Ptpn11(E76K) mutation has non-lineage-specific effects on malignant transformation of hematopoietic cells and initiates acute leukemias at various stages of hematopoiesis. 21930766

2011

dbSNP: rs1239681664
rs1239681664
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE Association of an MDR1 gene (C3435T) polymorphism with acute leukemia in India. 21133625

2010

dbSNP: rs13181
rs13181
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE The effect of XPD/ERCC2 Lys751Gln polymorphism on acute leukemia risk: a systematic review and meta-analysis. 24486506

2014

dbSNP: rs1325757098
rs1325757098
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE The BDNF Val66Met polymorphism may contribute to development of depressive symptomatology in patients undergoing stressful life events, such as diagnosis of acute leukemia and preparation for HSCT. 22652301

2013

dbSNP: rs1470755915
rs1470755915
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE Here, we aimed to evaluate the association between genotype or allele of CYP2B6 516G>T SNP and acute leukemia and myelodysplastic syndrome (MDS). 20878158

2011

dbSNP: rs1532268
rs1532268
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE This study tested the hypothesis that maternal folic acid supplementation before or during pregnancy reduces AL risk, accounting for the SNPs rs1801133 (C677T) and rs1801131 (A1298C) in MTHFR and rs1801394 (A66G) and rs1532268 (C524T) in MTRR, assumed to modify folate metabolism. 22706675

2012

dbSNP: rs1799929
rs1799929
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 GeneticVariation BEFREE Association between rs1799929 and decreased AL risk was found in the co-dominant (OR 0.82, 95% CI 0.70-0.97), homozygous (OR 0.65, 95% CI 0.46-0.93), heterozygous (OR 0.71, 95% CI 0.51-1.00), and the recessive model (OR 0.68, 95% CI 0.49-0.94) in the Caucasian group. 30896661

2019