SNP information rs10504861
Normal allele: CC
rs10504861 is a SNP located on chromosome 8q21 that has been found to be associated with an increased incidence of migraine without aura in whole-genome association studies.
Polymorphism rs10504861 is related to topics like this:
Migraine affects a significant portion of the adult population in most countries, with a higher...
Research and publications:
24852292 Selectivity in genetic association with sub-classified migraine in women.
26231841 Association of genetic loci for migraine susceptibility in the she people of China.
28079315 Migraine Susceptibility Genes in Han Chinese of Fujian Province.
Thrombophilia, an increased tendency to form abnormal blood clots that can obstruct blood vessels,...
Despite being often overlooked, the brain possesses an impressive ability to restrict the creation...
Abnormally high blood pressure in the arteries, which transport blood from the heart to the rest of...