Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
0.720 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
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
0.720 GeneticVariation BEFREE The five alleles were previously identified as being associated with migraine in a Western population, but it was not known if this association would hold in a She population. rs4379368 is in the succinic HMG coenzyme A transferase (C7orf10) gene; rs10504861 is near the matrix metallopeptidase 16 (MMP16) gene; rs10915437 is near the adherens junctions associated protein 1 (AJAP1) gene; rs12134493 is upstream of the tetraspanin 2 (TSPAN2) gene; and rs13208321 is within the four and a half LIM domains protein 5 (FHL5) gene. 26231841 2015
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
0.720 GeneticVariation GWASCAT Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013