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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 762 Black African ancestry individuals, 133 Mixed ancestry individuals, 94 Black African or Mixed ancestry individuals, 515 African American individuals.
The effect
Each copy of the G allele shifted the measure 0.277 lower (95% confidence interval 0.2-0.35); p = 4 × 10−13.
How common The G allele had a frequency of about 33% in the people studied.
Where it sits Chromosome 10, band 10q23.33 — between genes, 8.4 kb from CYP2C9.
What each result means
A/ANo copy of the version the research linked to Stable warfarin dose. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Stable warfarin dose. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Stable warfarin dose. That is the strongest link of the three results. A link in a study is not a diagnosis.
Blood advances · 2024 · PMID 39163621 · open access
Questions about rs58800757
What is rs58800757?
rs58800757 is a single position in the genome, in or near the near CYP2C9 gene. Published research associates it with stable warfarin dose. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs58800757 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 rs58800757 come from?
GWAS Catalog, Blood advances 2024, PMID:39163621. 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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