CFDP1 · rs8046697
Where this position leads
Condition: Blood Pressure
What the study found
Who was studied 526,001 European ancestry individuals.
The effect Each copy of the T allele shifted the measure 0.137 lower (95% confidence interval 0.094-0.179); p = 3 × 10−10.
Where it sits Chromosome 16, band 16q23.1 — in an intron of CFDP1.
rs8046697 is a single position in the genome, in or near the CFDP1 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, Investigative ophthalmology & visual science 2022, PMID:35762941. 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 (rs8046697). MyGeneLog™. https://www.mygenelog.com/variants/rs8046697