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Who was studied 38,609 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.045 lower (95% confidence interval 0.031-0.059); p = 7 × 10−10.
How common The A allele had a frequency of about 9% in the people studied.
Where it sits Chromosome 3, band 3q25.1 — in an intron of LINC01214.
What each result means
A/ATwo copies of the version the research linked to Adiponectin levels. 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 Adiponectin levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Adiponectin levels. This is the starting point the study compared everyone against.
rs7617025 is a single position in the genome, in or near the LINC01214 gene. Published research associates it with adiponectin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7617025 linked to?
On MyGeneLog this position is linked to Adiponectin Levels. The research behind each link, and its sources, are set out on that condition page.
Does having rs7617025 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 rs7617025 come from?
GWAS Catalog, HGG advances 2024, PMID:37859345. 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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