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Who was studied 3,037,499 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.00885 lower (95% confidence interval 0.0065-0.0112); p = 2 × 10−13.
How common The A allele had a frequency of about 75% in the people studied.
Where it sits Chromosome 2, band 2q14.3 — between genes, 88.7 kb from LINC01826.
What each result means
A/ATwo copies of the version the research linked to Educational attainment. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Educational attainment. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Educational attainment. This is the starting point the study compared everyone against.
Nature genetics · 2022 · PMID 35361970 · open access
Questions about rs58996896
What is rs58996896?
rs58996896 is a single position in the genome, in or near the near LINC01826 gene. Published research associates it with educational attainment. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs58996896 linked to?
On MyGeneLog this position is linked to Educational Attainment. The research behind each link, and its sources, are set out on that condition page.
Does having rs58996896 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 rs58996896 come from?
GWAS Catalog, Nature genetics 2022, PMID:35361970. 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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