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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 862 European ancestry cases, 17,021 European ancestry controls, 127 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 43 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 36 Asian ancestry cases, 734 Asian ancestry controls, 8 Native American ancestry cases, 34 Native American ancestry controls, 4 cases, 216 controls.
The effect
Each copy of the A allele carried 455.40 times the odds of Hemorrhagic stroke (95% confidence interval 50.992149254560125-4067.0053863877174); p = 4 × 10−8.
Where it sits Chromosome 7, band 7p22.3 — between genes, 68.4 kb from FOXL3.
What each result means
A/ATwo copies of the version the research linked to Hemorrhagic stroke. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Hemorrhagic stroke. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Hemorrhagic stroke. This is the starting point the study compared everyone against.
rs141857337 is a single position in the genome, in or near the near FOXL3 gene. Published research associates it with hemorrhagic stroke. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs141857337 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 rs141857337 come from?
GWAS Catalog, Stroke 2022, PMID:34727735. 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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