migraine with aura Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
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 http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:10024
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20 genes associated with the disease migraine with aura in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
TRPM8 transient receptor potential cation channel, subfamily M, member 8 1.31635
ADARB2 adenosine deaminase, RNA-specific, B2 (non-functional) 1.25477
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase 1.21019
VSTM4 V-set and transmembrane domain containing 4 1.19386
CTIF CBP80/20-dependent translation initiation factor 1.14463
LIMCH1 LIM and calponin homology domains 1 1.14463
GFRA1 GDNF family receptor alpha 1 1.10764
CHRM2 cholinergic receptor, muscarinic 2 1.07599
ACTN4 actinin, alpha 4 1.07599
SMYD3 SET and MYND domain containing 3 1.02476
SLC35D2 solute carrier family 35 (UDP-GlcNAc/UDP-glucose transporter), member D2 1.02476
BPIFC BPI fold containing family C 0.986376
FBN2 fibrillin 2 0.971169
NBEA neurobeachin 0.971169
LRP1 low density lipoprotein receptor-related protein 1 0.946163
FOXP1 forkhead box P1 0.807358
KSR2 kinase suppressor of ras 2 0.67359
MRVI1 murine retrovirus integration site 1 homolog 0.649249
PRDM16 PR domain containing 16 0.59854
SORBS1 sorbin and SH3 domain containing 1 0.511215