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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 997 European ancestry individuals; replicated in 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.63 lower (95% confidence interval 0.48-0.78); p = 5 × 10−16.
Where it sits Chromosome 14, band 14q22.3 — a missense change in FBXO34.
What each result means
C/CTwo copies of the version the research linked to Galectin-3 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Galectin-3 levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Galectin-3 levels. This is the starting point the study compared everyone against.
Nature communications · 2017 · PMID 28240269 · open access
Questions about rs35070799
What is rs35070799?
rs35070799 is a single position in the genome, in or near the FBXO34 gene. Published research associates it with galectin-3 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs35070799 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 rs35070799 come from?
GWAS Catalog, Nature communications 2017, PMID:28240269. 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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