Migraine with aura Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon. (Human Disease Ontology, DOID_10024)
External Link https://www.ebi.ac.uk/gwas/search?query=Migraine with aura
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Genes

15 genes associated with the Migraine with aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
TRPM8 transient receptor potential cation channel, subfamily M, member 8 0.342586
ADARB2 adenosine deaminase, RNA-specific, B2 (non-functional) 0.280662
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase 0.238523
VSTM4 V-set and transmembrane domain containing 4 0.220915
LIMCH1 LIM and calponin homology domains 1 0.165905
CTIF CBP80/20-dependent translation initiation factor 0.165905
GFRA1 GDNF family receptor alpha 1 0.129504
ACTN4 actinin, alpha 4 0.104568
LOC102723445 uncharacterized LOC102723445 0.085234
SMYD3 SET and MYND domain containing 3 0.070053
SLC35D2 solute carrier family 35 (UDP-GlcNAc/UDP-glucose transporter), member D2 0.070053
BPIFC BPI fold containing family C 0.048624
LOC101927558 uncharacterized LOC101927558 0.048624
FBN2 fibrillin 2 0.042592
NBEA neurobeachin 0.042592