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Migraine

near LINC02312 · rs117797734

Where this position leads

Condition: Migraine

rs117797734 Condition: Migraine Migraine Condition rs117797734 rs117797734 near LINC023…

What the study found

Who was studied 167 Portuguese ancestry cases, 174 Portuguese ancestry controls.

The effect Each copy of the T allele carried 7.40 times the odds of Migraine (95% confidence interval 4.202-13.05); p = 4 × 10−12.

Where it sits Chromosome 14, band 14q32.2 — between genes, 54 kb from LINC02312.

What each result means

C/C No copy of the version the research linked to Migraine. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Migraine. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Migraine. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source
Novel Potential Risk Loci for Migraine in the Portuguese Population
De Marco R, Pucci K, Santos M, Gil-Gouveia R, Cavadas B, Sousa A, Alves-Ferreira M, Azevedo L, Lemos C, Dias A
International journal of molecular sciences · 2026 · PMID 42352890 · open access

Questions about rs117797734

What is rs117797734?

rs117797734 is a single position in the genome, in or near the near LINC02312 gene. Published research associates it with migraine. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs117797734 linked to?

On MyGeneLog this position is linked to Migraine. The research behind each link, and its sources, are set out on that condition page.

Does having rs117797734 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs117797734 come from?

GWAS Catalog, International journal of molecular sciences 2026, PMID:42352890. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Migraine (rs117797734). MyGeneLog™. https://www.mygenelog.com/variants/rs117797734

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