Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Our objective was to determine the association between the methylenetetrahydrofolate reductase polymorphisms (C677T and A1298C) and the risk of developing acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CML), acute myeloid leukemia (AML), and multiple myelomas (MM) in Latinos. 31188929

2019

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Methylenetetrahydrofolate Reductase Gene C677T and A1298C Polymorphic Sequence Variations Influences the Susceptibility to Chronic Myeloid Leukemia in Kashmiri Population. 31396477

2019

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE The CT and TT genotypes of the MTHFR 6</span>77 C>T polymorphism were associated with an increased risk of developing CML (odds ratio (OR) = 1.556, 95% confidence interval (CI) = 1.017-2.381, p value = 0.041, and OR = 1.897, 95% CI = 1.046-3.44, p value = 0.035, respectively). 25510667

2015

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE For MTHFR C677T (dbSNP: rs1801133, C>T), though the pooled ORs were not significant in the overall population, all the ORs greater than 1 suggested an increased risk of CML for carriers of the risk allele. 24379141

2014

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE MTHFR A1298C and C677T gene polymorphisms and susceptibility to chronic myeloid leukemia in Egypt. 24966971

2014

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE In conclusion, our study revealed that MTHFR-C677T and -A1298C polymorphisms could not be considered as genetic risk factors for CML in Egyptians. 24338216

2014

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE The findings provide evidence that C677T and A1298C polymorphisms are risk factors for CML risk. 25080853

2014

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE The aim of this case-control study was to evaluate the association of the C677T MTHFR gene polymorphism with acute myeloid leukaemia (AML), acute lymphoblastic leukaemia (ALL), chronic myeloid leukaemia (CML) and chronic lymphocytic leukaemia (CLL). 22441130

2012

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Association between methylenetetrahydrofolate reductase polymorphism C677T and risk of chronic myeloid leukemia in Serbian population. 22132838

2012

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE We conducted a case-control study analyzing the prevalence of the polymorphisms MTHFR C677T, MTHFR A1298C, del{GSTM1}, del{GSTT1}, and haptoglobin in 105 patients with chronic myeloid leukemia (CML) and 273 healthy controls, using PCR-based methods. 22576927

2012

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Our results demonstrate that the MTHFR 1298CC homozygote variant is strongly associated with an increased risk of CML, while MTHFR C677T does not significantly affect the risk of CML. 17156840

2007

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE In this study we describe the genotyping of the MTHFR C677T polymorphism by melting curve analysis with the LightCycler in a case-controlled study of patients with acute lymphocytic leukemia (ALL), myelogenous leukemia (AML), and chronic myelogenous leukemia (CML), and assess the effect of this common polymorphism on the leukemia risk in adult patients in Turkey. 15068389

2003