PKN2-AS1 · rs12139208
Where this position leads
Condition: Intraocular Pressure
What the study found
Who was studied 139,555 European ancestry individuals.
The effect Each copy of the T allele shifted the measure 0.08 higher (95% confidence interval 0.055-0.105); p = 9 × 10−10.
How common The T allele had a frequency of about 38% in the people studied.
Where it sits Chromosome 1, band 1p22.3 — in an intron of PKN2-AS1.
rs12139208 is a single position in the genome, in or near the PKN2-AS1 gene. Published research associates it with intraocular 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 Intraocular 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 genetics 2018, PMID:29785010. 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.
Intraocular pressure (rs12139208). MyGeneLog™. https://www.mygenelog.com/variants/rs12139208