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Who was studied 139,555 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.16 higher (95% confidence interval 0.11-0.21); p = 5 × 10−12.
How common The G allele had a frequency of about 92% in the people studied.
Where it sits Chromosome 22, band 22q11.21 — in the 5′ untranslated region of GNB1L.
What each result means
A/ANo copy of the version the research linked to Intraocular pressure. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Intraocular pressure. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Intraocular pressure. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2018 · PMID 29785010 · open access
Questions about rs17534001
What is rs17534001?
rs17534001 is a single position in the genome, in or near the GNB1L 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.
What conditions is rs17534001 linked to?
On MyGeneLog this position is linked to Intraocular Pressure. The research behind each link, and its sources, are set out on that condition page.
Does having rs17534001 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 rs17534001 come from?
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.
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