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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 21,758 European ancestry individuals; replicated in 9,173 individuals.
The effect
Each copy of the T allele shifted the measure 0.134 lower; p = 7 × 10−18.
How common The T allele had a frequency of about 93% in the people studied.
Where it sits Chromosome 19, band 19p13.3 — in an intron of FUT3.
What each result means
C/CNo copy of the version the research linked to E-selectin levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to E-selectin levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to E-selectin levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs150092813 is a single position in the genome, in or near the FUT3 gene. Published research associates it with e-selectin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs150092813 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 rs150092813 come from?
GWAS Catalog, Nature metabolism 2020, PMID:33067605. 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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