Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397507444
rs397507444
MTHFR
0.050 GeneticVariation BEFREE Genotypic results indicated a non-significant increase in frequencies of CT and TT in C667T SNP in migraine patients with control (52 and 10% vs. 42 and 7%: p > 0.05), but CC genotype in A1298C was found to be a risk factor in migraine patients than controls (30 vs. 17% respectively: p < 0.05). 29427165

2018
dbSNP: rs397507444
rs397507444
MTHFR
0.050 GeneticVariation BEFREE We aimed to investigate the possible association between MTHFR gene rs4846049, C677T, and A1298C polymorphisms and the risk of migraine in Iranian population. 29379315

2018
dbSNP: rs397507444
rs397507444
MTHFR
0.050 GeneticVariation BEFREE MTHFR gene variants C677T and A1298C seem to be related to an increased risk of migraine. 17927652

2007
dbSNP: rs397507444
rs397507444
MTHFR
0.050 GeneticVariation BEFREE We found a trend toward an increased risk of migraine in subjects carrying a homozygous mutant genotype for MTHFR C677T and MTHFR A1298C polymorphisms. 16686913

2006
dbSNP: rs397507444
rs397507444
MTHFR
0.050 GeneticVariation BEFREE Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk. 12654508

2003