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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 3,521 Chinese ancestry individuals, European individuals (see Wu 2013)..
The effect
Each copy of the G allele shifted the measure 0.024 higher (95% confidence interval 0.016-0.032); p = 8 × 10−11.
Where it sits Chromosome 10, band 10q24.31 — in an intron of HIF1AN.
What each result means
A/ANo copy of the version the research linked to Palmitoleic acid (16:1n-7) levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Palmitoleic acid (16:1n-7) levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Palmitoleic acid (16:1n-7) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Journal of lipid research · 2017 · PMID 28298293 · open access
Questions about rs10883511
What is rs10883511?
rs10883511 is a single position in the genome, in or near the HIF1AN gene. Published research associates it with palmitoleic acid (16:1n-7) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10883511 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 rs10883511 come from?
GWAS Catalog, Journal of lipid research 2017, PMID:28298293. 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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