migraine with aura Gene Set

Dataset GWASdb 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 http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002077
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20 genes associated with the migraine with aura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
TRPM8 transient receptor potential cation channel, subfamily M, member 8 1.15352
ADARB2 adenosine deaminase, RNA-specific, B2 (non-functional) 1.09906
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase 1.05869
VSTM4 V-set and transmembrane domain containing 4 1.04365
CTIF CBP80/20-dependent translation initiation factor 1.00059
LIMCH1 LIM and calponin homology domains 1 1.00059
GFRA1 GDNF family receptor alpha 1 0.969142
CHRM2 cholinergic receptor, muscarinic 2 0.942765
ACTN4 actinin, alpha 4 0.942765
SMYD3 SET and MYND domain containing 3 0.899912
SLC35D2 solute carrier family 35 (UDP-GlcNAc/UDP-glucose transporter), member D2 0.899912
BPIFC BPI fold containing family C 0.868241
FBN2 fibrillin 2 0.855449
NBEA neurobeachin 0.855449
LRP1 low density lipoprotein receptor-related protein 1 0.833415
FOXP1 forkhead box P1 0.703184
KSR2 kinase suppressor of ras 2 0.577224
MRVI1 murine retrovirus integration site 1 homolog 0.554075
PRDM16 PR domain containing 16 0.508471
SORBS1 sorbin and SH3 domain containing 1 0.43652