near LINC01819 · rs76099932
Where this position leads
Condition: Blood Pressure
What the study found
Who was studied 349,328 British ancestry individuals; replicated in 144,022 European ancestry,African ancestry,Asian ancestry individuals.
The effect Each copy of the G allele shifted the measure 0.03 higher (95% confidence interval 0.022-0.038); p = 3 × 10−15.
Where it sits Chromosome 2, band 2p21 — between genes, 32.7 kb from LINC01819.
rs76099932 is a single position in the genome, in or near the near LINC01819 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.
On MyGeneLog this position is linked to Blood Pressure. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, Nature medicine 2024, PMID:38459180. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Diastolic blood pressure (rs76099932). MyGeneLog™. https://www.mygenelog.com/variants/rs76099932