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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 2,559 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.34 lower (95% confidence interval 0.24-0.44); p = 1 × 10−12.
How common The A allele had a frequency of about 11% in the people studied.
Where it sits Chromosome 19, band 19p13.3 — between genes, 0 kb from FUT6.
What each result means
A/ATwo copies of the version the research linked to N-glycan 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 N-glycan levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to N-glycan levels. This is the starting point the study compared everyone against.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs3760776
What is rs3760776?
rs3760776 is a single position in the genome, in or near the NRTN gene. Published research associates it with n-glycan levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What do people read about alongside rs3760776?
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (1 papers), vitamins and nutrient levels (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs3760776 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 rs3760776 come from?
GWAS Catalog, PLoS Genet 2010, PMID:21203500. 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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Quoting this page
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