|
rs1835740
|
|
|
0.860 |
GeneticVariation |
BEFREE |
Our data indicates that rs1835740 and MTDH might be involved in neurovascular headaches in general whilst rs2651899 is specifically related to migraine.
|
30382894 |
2018 |
|
rs1835740
|
|
|
0.860 |
GeneticVariation |
BEFREE |
We report significant influence of rs1835740, LRP1 rs11172113 and PRDM16 rs2651899 polymorphisms on migraine susceptibility in the North Indian population.
|
24266335 |
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 |
|
rs1835740
|
|
|
0.860 |
GeneticVariation |
BEFREE |
Carriers of the rs1835740 variant showed a non-significant tendency towards having a higher frequency of aura symptoms and a non-significant tendency towards milder migraine headache characteristics and fewer accompanying symptoms.
|
22103325 |
2012 |
|
rs1835740
|
|
|
0.860 |
GeneticVariation |
BEFREE |
Recently, a clinic-based genome-wide association study for migraine reported a functionally relevant risk variant (SNP rs1835740), involved in glutamate homeostasis, which showed a significant association with MA.
|
22908361 |
2012 |
|
rs1835740
|
|
A |
0.860 |
GeneticVariation |
GWASDB |
To our knowledge, our data establish rs1835740 as the first genetic risk factor for migraine.
|
20802479 |
2010 |
|
rs1835740
|
|
|
0.860 |
GeneticVariation |
BEFREE |
To our knowledge, our data establish rs1835740 as the first genetic risk factor for migraine.
|
20802479 |
2010 |
|
rs1835740
|
|
A |
0.860 |
GeneticVariation |
GWASCAT |
To our knowledge, our data establish rs1835740 as the first genetic risk factor for migraine.
|
20802479 |
2010 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
BEFREE |
To further check if these variants differ by ethnicity, three single nucleotide polymorphisms (SNPs) (rs4379368, rs10504861and rs11172113) were genotyped here to find association with migraine susceptibility from North Indian population.
|
31505242 |
2019 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
GWASCAT |
Detection and interpretation of shared genetic influences on 42 human traits.
|
27182965 |
2016 |
|
rs11172113
|
|
T |
0.850 |
GeneticVariation |
GWASCAT |
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
|
27322543 |
2016 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
BEFREE |
To further replicate the GWAS findings, we investigated the 3 variants rs2651899 (1p36.32, PRDM16), rs10166942 (2q37.1, TRPM8), and rs11172113 (12q13.3, LRP1) for their association with migraine in the Chinese Han population.
|
24666033 |
2014 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
BEFREE |
We report significant influence of rs1835740, LRP1 rs11172113 and PRDM16 rs2651899 polymorphisms on migraine susceptibility in the North Indian population.
|
24266335 |
2014 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
BEFREE |
The meta-analysis confirmed the previous three genome-wide significant associated SNPs (rs2651899, rs10166942 and rs11172113</span>) to confer risk of migraine.
|
23294458 |
2013 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
GWASCAT |
Genome-wide meta-analysis identifies new susceptibility loci for migraine.
|
23793025 |
2013 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
GWASDB |
Genome-wide meta-analysis identifies new susceptibility loci for migraine.
|
23793025 |
2013 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis identifies susceptibility loci for migraine without aura.
|
22683712 |
2012 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
GWASDB |
Genome-wide association analysis identifies susceptibility loci for migraine without aura.
|
22683712 |
2012 |
|
rs11172113
|
|
|
0.850 |
GeneticVariation |
BEFREE |
In a population-based genome-wide analysis including 5,122 migraineurs and 18,108 non-migraineurs, rs2651899 (1p36.32, PRDM16), rs10166942 (2q37.1, TRPM8) and rs11172113 (12q13.3, LRP1) were among the top seven associations (P < 5 × 10(-6)) with migraine.
|
21666692 |
2011 |
|
rs11172113
|
|
T |
0.850 |
GeneticVariation |
GWASCAT |
In a population-based genome-wide analysis including 5,122 migraineurs and 18,108 non-migraineurs, rs2651899 (1p36.32, PRDM16), rs10166942 (2q37.1, TRPM8) and rs11172113 (12q13.3, LRP1) were among the top seven associations (P < 5 × 10(-6)) with migraine.
|
21666692 |
2011 |
|
rs11172113
|
|
T |
0.850 |
GeneticVariation |
GWASDB |
In a population-based genome-wide analysis including 5,122 migraineurs and 18,108 non-migraineurs, rs2651899 (1p36.32, PRDM16), rs10166942 (2q37.1, TRPM8) and rs11172113 (12q13.3, LRP1) were among the top seven associations (P < 5 × 10(-6)) with migraine.
|
21666692 |
2011 |
|
rs4379368
|
|
|
0.830 |
GeneticVariation |
BEFREE |
This study was able to associate the role of rs4379368 SNP with migraine susceptibility and suggested that genotype CT in rs4379368 SNP could be a possible genetic marker for MA.
|
31505242 |
2019 |
|
rs12134493
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Previous studies have identified significant associations of the <i>TSPAN2</i> single nucleotide polymorphisms (SNPs) rs12134493 and rs2078371 with migraine in Western populations; however, these associations need to be confirmed in the Chinese Han population.
|
30258394 |
2018 |
|
rs12134493
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Five single-nucleotide polymorphisms (SNPs) (rs4379368, rs10504861, rs10915437, rs12134493 and rs13208321) were recently identified in a Western population with migraine.
|
28079315 |
2017 |
|
rs4379368
|
|
|
0.830 |
GeneticVariation |
BEFREE |
The CT genotype of rs4379368 was more common in migraine patients with aura (75%) than in migraine patients without aura (47.9%) and controls (48.5%) (p<0.05), and the TT genotype of rs10504861 was more common in migraine patients with aura than in controls (8.3% vs. 0.5%) (p<0.05).
|
28079315 |
2017 |