Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Expert opinion: Determination of MTHFR C677T polymorphisms as well as measurement of homocysteine concentrations may be useful to migraine patients, particularly those suffering from migraine with aura. 30451038

2019

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE In adult studies the MTHFR C677T polymorphism has been associated with an increased risk of migraine, but little research has been done in this area in children. 30170616

2018

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Present data provide evidence for the association of rs4846049 and C677T polymorphisms in the MTHFR gene and migraine. 29379315

2018

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE In this genetic association study, the prevalence of the functionally relevant polymorphisms C677T in the MTHFR gene and I/D polymorphism in the ACE gene was compared in 420 patients with migraine vs 258 migraine-free controls using a chi-square statistic and binary logistic regression. 27483173

2016

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE We conclude that the C677T MTHFR polymorphism, responsible for a reduction of the MTHFR activity in folate metabolism, may act as a genetic susceptibility factor for migraine, MA in particular among the subjects of Asian descent. 24183284

2014

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE We have analyzed clinical and electrophysiological characteristics of 83 patients with migraine (migraine with aura (MA), 19 patients, and migraine without aura (MO), 64 patients, according to the ICHD-II (2003)) taking into account their genotypes of C677T variant of MTHFR. 23915182

2013

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Our data suggested that MTHFR C677T polymorphism plays a role in Chinese migraine susceptibility, especially in MO. 23811028

2013

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Frequency of the C677T variant of the methylenetetrahydrofolate reductase (MTHFR) gene in patients with migraine with or without aura - a preliminary report. 23161188

2013

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE BMIs were significantly lower in the control than the migraine group (p = 0.021); however, an association between the C677T variant and BMI was not found (p = 0.787) in the migraine group. 23975093

2013

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE By multivariate logistic stepwise regression analysis, type of migraine, regular and sufficient dietary intake, and methylenetetrahydrofolate reductase (MTHFR) C677T (rs1801133) and dopamine D2 receptor (DRD2) C939T (rs6275) polymorphisms were selected as significant factors that contribute independently to the development from migraine to MOH (P < 0.05). 22290307

2013

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Using the multivariate analysis, three gene polymorphisms including monoamine oxidase A (MAOA) T941G, methylenetetrahydrofolate reductase (MTHFR) C677T, and tumor necrosis factor beta (TNF-β) G252Α, and the neuroticism and conscientiousness scores in NEO-FFI were selected as significant factors that independently contributed to the pathogenesis of migraine. 22193458

2012

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE When the vitamin-treated group was stratified by genotype, the C allele carriers of the MTHFR C677T variant showed a higher reduction in homocysteine levels (P<0.001), severity of pain in migraine (P=0.01) and percentage of high migraine disability (P=0.009) compared with those with the TT genotypes. 22926161

2012

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Individuals with migraine (n = 447) were selected from the Depression Case Control (DeCC) study to investigate the association between migraine and MTHFR C677T single nucleotide polymorphism (SNP) rs1801133 using an additive model compared to non-migraineurs adjusting for depression status. 21635773

2011

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Homozygosity for the methylenetetrahydrofolate reductase (MTHFR) 677C>T mutation (MTHFR TT) has been linked to an increased risk for stroke, coronary artery disease, and migraine headaches. 21270470

2011

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Thirteen studies investigated the association between the MTHFR 677C>T polymorphism and migraine. 19925624

2010

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE MTHFR 677C->T and ACE D/I polymorphisms and migraine attack frequency in women. 19673907

2010

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Association of von Willebrand factor activity with ACE I/D and MTHFR C677T polymorphisms in migraine. 19298544

2009

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE No significant differences in genotype and allelic frequencies of MTHFR C677T polymorphism were found on comparing migraine patients with either disease controls or healthy controls. 19081115

2009

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Association of the C677T polymorphism in the MTHFR gene with migraine: a meta-analysis. 17714520

2009

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Thus, we conclude that the C677T MTHFR polymorphism, responsible for a reduction of the MTHFR activity in folate metabolism, is not a major genetic susceptibility factor for migraine in the Portuguese population. 18957721

2008

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Migraine mediates the influence of C677T MTHFR genotypes on ischemic stroke risk with a stroke-subtype effect. 17962595

2007

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE MTHFR gene variants C677T and A1298C seem to be related to an increased risk of migraine. 17927652

2007

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE The MTHFR C677T genotype has been associated with increased risk of migraine, particularly of migraine with aura (MA) in selected clinical samples and with elevated homocysteine. 17300365

2007

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Mutations in 3 different genes responsible for familial hemiplegic migraine, a monogenetic subtype of migraine with aura, and the MTHFR C677T polymorphism in common forms of migraine are clear examples. 16866710

2006

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Migraine and MTHFR C677T genotype in a population-based sample. 16365871

2006