Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Colorectal cancer and the methylenetetrahydrofolate reductase 677C -> T and methionine synthase 2756A -> G polymorphisms: a study of 2,168 case-control pairs from the JANUS cohort. 15598777

2004

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Colo-rectal cancer risk is decreased in subjects homozygous for a common variant (C677T) of the gene coding for this enzyme, suggesting that DNA synthesis and repair may be 'enhanced' in these individuals. 15831129

2004

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE C677T and A1298C mutations in the MTHFR gene and survival in colorectal cancer. 20076818

2009

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE A common C to T transition (C677T) in the MTHFR gene is reported to reduce the risk for colorectal cancer and acute lymphocytic leukemia in homozygotes (TTs). 11408344

2001

dbSNP: rs1801133
rs1801133
0.100 GeneticVariation BEFREE After excluding 13 studies according to their heterogeneity and publication bias, rs1801133 polymorphism was found to reduce the risks of CRC significantly (OR =0.96, 95% CI =0.94-0.99). 29089462

2017

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Although MTHFR C677T was associated with increased risks of colorectal cancer, leukemia, and gastric cancer, our pooled data suggest no evidence for a major role of MTHFR C677T in the carcinogenesis of childhood acute lymphoblastic leukemia. 20409583

2010

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Although the mechanism responsible for the link between the C677T polymorphism and microsatellite instability was not apparent, this finding may provide a clue towards a better understanding of the pathogenesis of microsatellite instability in human colorectal cancer. 16819711

2006

dbSNP: rs397507444
rs397507444
0.100 GeneticVariation BEFREE Although the MTHFR A1298C polymorphism was not associated with OS in CRC, this polymorphism was associated with significantly shorter OS in rectal cancer. 28044213

2017

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Although the underlying mechanisms still remain to be clarified, epidemiological findings regarding MTHFR C677T polymorphism provide strong evidence that adequate folate status confers protection from colorectal cancer. 16128738

2005

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Association of MTHFR C677T polymorphisms and colorectal cancer risk in Asians: evidence of 12,255 subjects. 24193867

2014

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Association studies on the MTHFR polymorphisms (C677T and A1298C) in colorectal cancer (CRC) and colorectal adenoma have shown conflicting results. 17089070

2007

dbSNP: rs397507444
rs397507444
0.100 GeneticVariation BEFREE C667T and A1298C mutations represent a risk factor for colorectal cancer with an OR (odds ratio) = 2.13 (CI (0.51-8.91)) and 3 (CI(0.3-29.58), respectively, in homozygous patients. 17925917

2007

dbSNP: rs397507444
rs397507444
0.100 GeneticVariation BEFREE C677T and A1298C mutations in the MTHFR gene and survival in colorectal cancer. 20076818

2009

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Certain common polymorphisms within the MTHFR gene (C677T, A1298C) result in reduced enzymatic activity and have been associated with reduced risk for a variety of cancers such as acute lymphocytic leukemia, lung and colorectal cancer. 18804702

2008

dbSNP: rs397507444
rs397507444
0.100 GeneticVariation BEFREE Certain common polymorphisms within the MTHFR gene (C677T, A1298C) result in reduced enzymatic activity and have been associated with reduced risk for a variety of cancers such as acute lymphocytic leukemia, lung and colorectal cancer. 18804702

2008

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Consistent with the folate/methylation hypothesis, it was originally proposed that C677T may increase risk of CRC due to hypomethylation of oncogenes. 16933051

2006

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Different polymorphisms have been described for this enzyme, the most studied being the C677T, which has been shown to be associated with predisposition to colorectal cancer in patients who consume a high alcohol diet. 15033905

2004

dbSNP: rs397507444
rs397507444
0.100 GeneticVariation BEFREE Different roles of MTHFR C677T and A1298C polymorphisms in colorectal adenoma and colorectal cancer: a meta-analysis. 17089070

2007

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE DPYD*2A and MTHFR C677T predict toxicity and efficacy, respectively, in patients on chemotherapy with 5-fluorouracil for colorectal cancer. 29134491

2018

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Evidence from the current meta-analysis indicated that the C677T polymorphism is not associated with CRC risk in Asian populations. 26745044

2015

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Females who were heterozygous or homozygous for the C677T MTHFR polymorphism were at increased risk of developing CIMP+ CRC (odds ratio 2.17, 95% confidence interval 1.03-4.57; p=0.037). 12427779

2002

dbSNP: rs397507444
rs397507444
0.100 GeneticVariation BEFREE Functional variants in the methylenetetrahydrofolate reductase (MTHFR) gene, including the 677C>T and 1298A>C polymorphisms, have been associated with a moderately reduced risk of several cancers, including colorectal cancers. 16217917

2005

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Functional variants in the methylenetetrahydrofolate reductase (MTHFR) gene, including the 677C>T and 1298A>C polymorphisms, have been associated with a moderately reduced risk of several cancers, including colorectal cancers. 16217917

2005

dbSNP: rs1801133
rs1801133
0.100 GeneticVariation BEFREE Further SNPs associated with CRC risk included several previously reported to be associated with cancer risk including ATM F858L [OR=1.48; 95% confidence interval (CI): 1.06-2.07] and P1054R (OR=1.42; 95% CI: 1.14-1.77) and MTHFR A222V (OR=0.82; 95% CI: 0.69-0.97). 17000706

2006

dbSNP: rs1801133
rs1801133
0.100 GeneticVariation BEFREE However, <i>MTHFR</i> rs1801133 G>A polymorphism confers a decreased risk to CRC. 28969008

2017