Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation BEFREE This research study showed that rs2651899 is a potential genetic marker for migraine susceptibility in MO and female subgroup at both genotypic and allelic level in the North Indian population and found that rs10166942 variant may be a potential marker for MA and male subgroup. 30635810

2019
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation BEFREE We infer strong positive selection, in agreement with ancient DNA showing high frequency of the allele in Europe 3,000 to 8,000 years ago. rs10166942 is important phenotypically because its ancestral allele is protective of migraine. 29723195

2018
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation GWASCAT Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. 27322543

2016
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation BEFREE On the other hand, TRPM8 rs10166942 and TGFBR2 rs7640543 variants did not have significant influence on migraine susceptibility in the North Indian population. 24266335

2014
dbSNP: rs10166942
rs10166942
TRPM8
0.870 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
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation BEFREE Recent genome-wide association studies (GWAS) have identified 3 loci in or near PRDM16 (1p36.32, rs2651899), LRP1 (12q13.3, rs11172113) and TRPM8 (2q37.1, rs10166942) in the population-based Women's Genome Health Study (WGHS) of migraine, and 2 loci in or near TRPM8 and LRP1 were repeated in European GWAS study. 24021092

2014
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025

2013
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation BEFREE The meta-analysis confirmed the previous three genome-wide significant associated SNPs (rs2651899, rs101</span>66942 and rs11172113) to confer risk of migraine. 23294458

2013
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation GWASDB Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712

2012
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation GWASCAT Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712

2012
dbSNP: rs10166942
rs10166942
TRPM8
0.870 GeneticVariation BEFREE The associations at rs2651899 and rs10166942 were specific for migraine compared with non-migraine headache. 21666692

2011
dbSNP: rs10166942
rs10166942
TRPM8
T 0.870 GeneticVariation GWASCAT The associations at rs2651899 and rs10166942 were specific for migraine compared with non-migraine headache. 21666692

2011
dbSNP: rs10166942
rs10166942
TRPM8
T 0.870 GeneticVariation GWASDB The associations at rs2651899 and rs10166942 were specific for migraine compared with non-migraine headache. 21666692

2011