Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE Our findings suggest that the MTHFR 677C>T and 1298A>C gene variants do not have a major influence on the susceptibility to pediatric ALL in the German population. 15921520

2005

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE The MTHFR C677T and A1298C polymorphisms and susceptibility to childhood acute lymphoblastic leukemia in Portugal. 16096524

2005

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE However, 677T allele was linked to a decrease risk of ALL [odds ratio (OR), 0.43; 95% confidence interval (CI), 0.22-0.86], whereas the 1298A>C polymorphism presents an elevated risk factor [OR, 2.01; 95% CI, 1.01-3.99] in non-White children. 16182363

2006

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE Although no consistent results on associations between MTHFR A 1298C polymorphism and ALL in the populations studied were obtained, the A1298C polymorphism, at least in Koreans, may be a genetic determinant among childhood ALL patients. 16886608

2006

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE A meta-analysis of case-control studies that investigated the association between the C677T and/or A1298C polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene and acute lymphoblastic leukemia (ALL) was carried out. 16897583

2006

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE Most studies found a strong association between the polymorphisms MTHFR, C677T or A1298C, and NQO1*2 or *3 and the risk of acute lymphoblastic leukemia (ALL). 17023046

2006

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE No association between the A1298C variant and susceptibility to both adult and childhood ALL was disclosed. 17035405

2006

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE DNA samples taken from patients with ALL and controls were analyzed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assays to detect the MTHFR C677T and A1298C mutations. 17970089

2007

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE No significant relation was found between MTHFR A1298C polymorphism and the risks of therapy induced complications or relapse rate in the studied ALL patients. 19923983

2010

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE We conducted a case-control study in 95 north Indian children with acute lymphoblastic leukemia (ALL) and 255 controls, to investigate the role of MTHFR C677T and A1298C polymorphisms as risk factors in the development of ALL. 20367562

2010

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE It has been suggested that two MTHFR polymorphisms, 677C>T and 1298A>C, influence risk of acute lymphoblastic leukemia (ALL). 20374270

2010

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE These results suggest that the MTHFR C677T, but not A1298C, polymorphism is a potential biomarker for childhood ALL risk. 21495160

2012

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE For the MTHFR A1298C polymorphism, no significant association with ALL susceptibility was observed in the pooled analyses. 21702646

2011

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE Seventy-two children with ALL and 109 age- and sex-matched healthy children from Western Iran were screened for MTHFR C677T and A1298C variants by using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). 22017305

2012

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE In total, 167 children with ALL were genotyped for methylenetetrahydrofolate dehydrogenase (MTHFD1) 1958G > A, methylenetetrahydrofolate reductase (MTHFR) 677C > T and 1298A > C and thymidylate synthase (TYMS) 2R > 3R polymorphisms. 22074251

2012

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE The genetic association studies (GAS) that investigated the association between ALL and the MTHFR C677T and A1298C gene variants have produced contradictory or inconclusive results. 22094326

2012

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE 5,10-methylenetetrahydrofolate reductase (MTHFR) variants, C677T and A1298C, have been reported to be associated with decreased risk of acute lymphoblastic leukemia (ALL). 22943282

2012

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE The A1298C polymorphism had an effect on ALL risk neither in adults (Dominant model: OR(FE)=0.95, 95% CI: 0.71-1.27, p=0.72) nor in children (Dominant model: OR(FE)=1.02, 95% CI: 0.87-1.21, p=0.77). 23061880

2012

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE In conclusion, MTHFR, C677T and A1298C polymorphisms do not seem to be good markers of MTX-related toxicity in pediatric ALL. 23089671

2013

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE In conclusion, the MTHFR C677T and A1298C haplotypes might be useful for monitoring adverse effects in childhood ALL maintenance therapy in Japanese patients. 23865834

2014

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE However, a significant association was detected between the MTHFR A1298C/ RFC G80A genotype and a nonpredisposition for ALL (P = 0.035). 24237708

2014

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE Two polymorphisms of the gene encoding MTHFR, C677T and A1298C, alter MTHFR enzyme activity and may be associated with ALL relapse. 24637499

2014

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE The aims of this study were to (a) to determine the prevalence of seven common genetic polymorphisms including those that affect the folate and/or thiopurine metabolic pathways, i.e. cyclin D1 (CCND1-G870A), γ-glutamyl hydrolase (GGH-C452T), methylenetetrahydrofolate reductase (MTHFR-C677T and MTHFR-A1298C), thymidylate synthase promoter (TYMS-TSER), thiopurine methyltransferase (TPMT*3A and TPMT*3C) and inosine triphosphate pyrophosphatase (ITPA-C94A), in Caucasian (n = 94, age < 20) and Vietnamese (n = 141, age < 16 years) childhood ALL and (b) to assess the impact of a multilocus genetic risk score (MGRS) on relapse-free survival (RFS) using a Cox proportional-hazards regression model. 25099492

2015

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE In a case-control study of 203 patients with ALL and 246 controls and meta-analysis in the Indian population, we showed an insignificant association of MTHFR C677T and A1298C genotypes with childhood and adult ALL. 25115513

2015

dbSNP: rs397507444
rs397507444
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE Our results suggest that the MTHFR C677T and A1298C polymorphisms may be potential biomarkers for ALL risk in Chinese populations, and studies with a larger sample size and wider population spectrum are required before definitive conclusions can be drawn. 25342508

2014