Normal allele: CC
Polymorphism rs10166942 is related to topics like this:
Research and publications:
22072275 Genetics of migraine in the age of genome-wide association studies.
22379397 Genetics of recurrent vertigo and vestibular disorders.
24021092 PRDM16 rs2651899 variant is a risk factor for Chinese common migraine patients.
26231841 Association of genetic loci for migraine susceptibility in the she people of China.
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.
34588893 PRDM16, LRP1 and TRPM8 genetic polymorphisms are risk factor for Pakistani migraine patients.