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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 100,453 Chinese Han ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.736 higher (95% confidence interval 0.58-0.89); p = 1 × 10−21.
How common The T allele had a frequency of about 79% in the people studied.
Where it sits Chromosome 3, band 3p24.1 — between genes, 6.2 kb from Y_RNA.
What each result means
C/CNo copy of the version the research linked to Pulse pressure (BMI adjusted). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Pulse pressure (BMI adjusted). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Pulse pressure (BMI adjusted). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2024 · PMID 39048560 · open access
Questions about rs9847595
What is rs9847595?
rs9847595 is a single position in the genome, in or near the near Y_RNA gene. Published research associates it with pulse pressure (bmi adjusted). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9847595 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 rs9847595 come from?
GWAS Catalog, Nature communications 2024, PMID:39048560. 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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