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Who was studied 1,028,980 European ancestry individuals; replicated in 62,047 African ancestry individuals, 21,843 African American individuals.
The effect
Each copy of the G allele shifted the measure 0.096 higher (95% confidence interval 0.066-0.126); p = 2 × 10−10.
Where it sits Chromosome 21, band 21q22.2 — in an intron of ERG.
What each result means
C/CNo copy of the version the research linked to Diastolic blood pressure. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Diastolic blood pressure. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Diastolic blood pressure. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2024 · PMID 38689001 · open access
Questions about rs2836554
What is rs2836554?
rs2836554 is a single position in the genome, in or near the ERG gene. Published research associates it with diastolic blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs2836554 linked to?
On MyGeneLog this position is linked to Blood Pressure. The research behind each link, and its sources, are set out on that condition page.
Does having rs2836554 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 rs2836554 come from?
GWAS Catalog, Nature genetics 2024, PMID:38689001. 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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