|
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Migraine and MTHFR C677T genotype in a population-based sample.
|
16365871 |
2006 |
|
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Migraine mediates the influence of C677T MTHFR genotypes on ischemic stroke risk with a stroke-subtype effect.
|
17962595 |
2007 |
|
rs752380770
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A280V polymorphism in the histamine H3 receptor as a risk factor for migraine.
|
21376262 |
2011 |
|
rs3794087
|
|
|
0.010 |
GeneticVariation |
BEFREE |
rs3794087 genotype and allelic variants were not related with the risk for migraine in Caucasian Spanish people.
|
24412224 |
2014 |
|
rs1835740
|
|
|
0.860 |
GeneticVariation |
BEFREE |
A large two-stage GWAS by Antilla et al. reported the minor allele of rs1835740 on 8q22.1 to be associated with common types of migraine.
|
21964821 |
2012 |
|
rs867770797
|
|
|
0.030 |
GeneticVariation |
BEFREE |
A recent association study has shown that the biallelic -231 G>A polymorphism of the EDNRA gene is associated to migraine in an elderly population.
|
16618267 |
2006 |
|
rs758454871
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Also, POLG mutations (eg, p.T851 A, p.N468D, p.Y831C, p.G517V, and p.P163S) can cause disease through impaired replication of mtDNA, including migraine.
|
24331360 |
2013 |
|
rs5498
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Although the independent risk factor constituted by this polymorphism in other ethnic groups requires further study, our studies raise the possibility of the development of ICAM1 K469E E allele-specific therapeutics for the prevention and treatment of migraine in the Chinese Han population.
|
25145994 |
2014 |
|
rs9566867
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Although the level of significance was significantly reduced when using the Fisher's exact test (as a result of the low count of cases with migraine), rs9566845 P = 1.4 × 10(-5) and rs9566867 P = 1.5 × 10(-5), this region remained the most prominent finding.
|
20528957 |
2010 |
|
rs3754701
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Although we find no significant association of any of the SNPs tested with migraine overall, we detected a nominally significant association (p=0.031) of the RAMP1 rs3754701 variant in male migraine subjects, although this is non-significant after Bonferroni correction for multiple testing.
|
23237777 |
2013 |
|
rs11542041
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Altogether, 134 Finnish CADASIL patients with p.Arg133Cys mutation were analysed for possible associations between the apolipoprotein E (APOE) genotype, angiotensinogen (AGT) p.Met268Thr polymorphism or neutral p.Ala202Ala NOTCH3 polymorphism and earlier first-ever stroke or migraine.
|
25819272 |
2015 |
|
rs137852642
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Altogether, 134 Finnish CADASIL patients with p.Arg133Cys mutation were analysed for possible associations between the apolipoprotein E (APOE) genotype, angiotensinogen (AGT) p.Met268Thr polymorphism or neutral p.Ala202Ala NOTCH3 polymorphism and earlier first-ever stroke or migraine.
|
25819272 |
2015 |
|
rs699
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Altogether, 134 Finnish CADASIL patients with p.Arg133Cys mutation were analysed for possible associations between the apolipoprotein E (APOE) genotype, angiotensinogen (AGT) p.Met268Thr polymorphism or neutral p.Ala202Ala NOTCH3 polymorphism and earlier first-ever stroke or migraine.
|
25819272 |
2015 |
|
rs1043994
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Altogether, 134 Finnish CADASIL patients with p.Arg133Cys mutation were analysed for possible associations between the apolipoprotein E (APOE) genotype, angiotensinogen (AGT) p.Met268Thr polymorphism or neutral p.Ala202Ala NOTCH3 polymorphism and earlier first-ever stroke or migraine.
|
25819272 |
2015 |
|
rs745738344
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Among the ten studies identified, the best evidence is available for the TNFα -308G>A and TNFβ 252A > G polymorphisms indicating no overall association with migraine.
|
22001640 |
2011 |
|
rs2271933
|
|
|
0.020 |
GeneticVariation |
BEFREE |
An HCRTR1 gene variant (rs2271933 G > A) leading to amino acid substitution (Ile408Val) has been associated with migraine and mood disorders.
|
30742846 |
2019 |
|
rs6313
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Association analysis of 5-HTTLPR variants, 5-HT2a receptor gene 102T/C polymorphism and migraine.
|
14668201 |
2004 |
|
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Association of the C677T polymorphism in the MTHFR gene with migraine: a meta-analysis.
|
17714520 |
2009 |
|
rs397507444
|
|
|
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 |
|
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Association of von Willebrand factor activity with ACE I/D and MTHFR C677T polymorphisms in migraine.
|
19298544 |
2009 |
|
rs6790925
|
|
|
0.810 |
GeneticVariation |
BEFREE |
At one extreme, SNPs rs6790925 (near TGFBR2) and rs2274316 (MEF2D) were not associated with migraine overall, MA, or MO but were selective for migraine sub-classified by the presence of one or more of the additional migraine features.
|
24852292 |
2014 |
|
rs2274316
|
|
|
0.820 |
GeneticVariation |
BEFREE |
At one extreme, SNPs rs6790925 (near TGFBR2) and rs2274316 (MEF2D) were not associated with migraine overall, MA, or MO but were selective for migraine sub-classified by the presence of one or more of the additional migraine features.
|
24852292 |
2014 |
|
rs712507
|
|
|
0.010 |
GeneticVariation |
BEFREE |
BDNF SNPs rs1519480, rs6265, rs712507, and rs12273363 were not significantly associated with migraine.
|
24708359 |
2015 |
|
rs12273363
|
|
|
0.010 |
GeneticVariation |
BEFREE |
BDNF SNPs rs1519480, rs6265, rs712507, and rs12273363 were not significantly associated with migraine.
|
24708359 |
2015 |
|
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 |