Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE Polymorphism in the methylenetetrahydrofolate reductase (C677T) gene and homocysteine levels: a comparison in Brazilian patients with coronary arterial disease, ischemic stroke and peripheral arterial obstructive disease. 18040753

2009

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE Our TDT analysis clearly demonstrates a lack of association between the T allele of the C677T mutation in MTHFR and cardiovascular artery disease, both for the general group and for different risk subgroups (smokers, hypertension, male sex, overweight and type A behaviour pattern) in the Spanish population. 12220440

2002

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE However, the results of most of the previous studies suggest that the C677T MTHFR mutation is not a significant risk factor for arterial disease. 10360632

1999

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients. 10477457

1999