Trait
Migraine with aura
A type of migraine in which there is an aura characterized by focal neurological phenomena that usually proceed, but may accompany or occur in the absence of, the headache. The symptoms of an aura may include fully reversible visual, sensory, and speech symptoms but not motor weakness. Visual symptoms may include flickering lights, spots and lines and/or loss of vision and/or unilateral sensory symptoms such as paresthesias or numbness. At least one of the symptoms of an aura develops gradually over 5 or more minutes and/or different symptoms occur in succession.
Summary
- Body system
- Abnormality of the nervous system
Read the genes linked to Migraine with aura, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test12 genes linked to Migraine with aura
Changes in these genes cause rare conditions in which Migraine with aura is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| SCN1Asodium voltage-gated channel alpha subunit 1 | Always | In 2 conditions |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Very often (80–99%) | In 2 conditions |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Very often (80–99%) | In 2 conditions |
| PRRT2proline rich transmembrane protein 2 | Very often (80–99%) | In 1 condition |
| COL4A1collagen type IV alpha 1 chain | Often (30–79%) | In 1 condition |
| NOTCH3notch receptor 3 | Often (30–79%) | In 1 condition |
| TREX1three prime repair exonuclease 1 | Sometimes (5–29%) | In 1 condition |
| CSNK1Dcasein kinase 1 delta | Not recorded | In 1 condition |
| EDNRAendothelin receptor type A | Not recorded | In 1 condition |
| ESR1estrogen receptor 1 | Not recorded | In 1 condition |
| KCNK18potassium two pore domain channel subfamily K member 18 | Not recorded | In 1 condition |
| TNFtumor necrosis factor | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks