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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 228 African American or Afro-Caribbean cases, 121,537 African American or Afro-Caribbean controls, 737 European ancestry cases, 449,997 European ancestry controls.
The effect
Each copy of the G allele shifted the measure 2.33 lower (95% confidence interval 2.28-2.38); p = 4 × 10−11.
How common The G allele had a frequency of about 100% in the people studied.
Where it sits Chromosome 6, band 6q15 — between genes, 96.8 kb from U3.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of Subarachnoid hemorrhage (PheCode 430.1) — no copies of the reported risk allele.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Subarachnoid hemorrhage (PheCode 430.1).
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Subarachnoid hemorrhage (PheCode 430.1) compared to the general population.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs185673589
What is rs185673589?
rs185673589 is a single position in the genome, in or near the near U3 gene. Published research associates it with subarachnoid hemorrhage (phecode 430.1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs185673589 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 rs185673589 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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