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SNP information rs10166942

RS10166942

Normal allele: CC

Polymorphism rs10166942 is related to topics like this:

CGRP migraine

Migraine affects a significant portion of the adult population in most countries, with a higher...


Research and publications:

  21666692   Genome-wide association study reveals three susceptibility loci for common migraine in the general population.

  22072275   Genetics of migraine in the age of genome-wide association studies.

  22379397   Genetics of recurrent vertigo and vestibular disorders.

  23294458   Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine.

  24021092   PRDM16 rs2651899 variant is a risk factor for Chinese common migraine patients.

  24674449   A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample.

  25388962   Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura.

  26231841   Association of genetic loci for migraine susceptibility in the she people of China.

  26747084   Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.

  28952330   Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan.

  29723195   Human local adaptation of the TRPM8 cold receptor along a latitudinal cline.

  30635810   rs2651899 variant is associated with risk for migraine without aura from North Indian population.

  31842742   TRPM8 genetic variant is associated with chronic migraine and allodynia.

  31873179   Reduced TRPM8 expression underpins reduced migraine risk and attenuated cold pain sensation in humans.

  34588893   PRDM16, LRP1 and TRPM8 genetic polymorphisms are risk factor for Pakistani migraine patients.

  35454329   Deciphering the Role of the rs2651899, rs10166942, and rs11172113 Polymorphisms in Migraine: A Meta-Analysis.

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