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Who was studied 5,708 European ancestry cases, 432,028 European ancestry controls; replicated in 3,989 cases, 226,643 controls.
The effect
Each copy of the C allele carried 1.35 times the odds of Myasthenia gravis (95% confidence interval 1.29-1.4); p = 3 × 10−25.
How common The C allele had a frequency of about 7% in the people studied.
Where it sits Chromosome 6, band 6p22.1 — between genes, 5 kb from TRIM31-AS1.
What each result means
C/CTwo copies of the version the research linked to Myasthenia gravis. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Myasthenia gravis. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Myasthenia gravis. This is the starting point the study compared everyone against.
Nature communications · 2024 · PMID 39537604 · open access
Questions about rs1264706
What is rs1264706?
rs1264706 is a single position in the genome, in or near the near TRIM31-AS1 gene. Published research associates it with myasthenia gravis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs1264706 linked to?
On MyGeneLog this position is linked to Myasthenia Gravis. The research behind each link, and its sources, are set out on that condition page.
Does having rs1264706 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 rs1264706 come from?
GWAS Catalog, Nature communications 2024, PMID:39537604. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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