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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 5,006 European ancestry individuals; replicated in 1,124 European ancestry individuals, 3,764 individuals.
The effect
Each copy of the C allele shifted the measure 0.03 ug/L lower (95% confidence interval 0.02-0.04); p = 7 × 10−15.
How common The C allele had a frequency of about 35% in the people studied.
Where it sits Chromosome 10, band 10q23.33 — in the 3′ untranslated region of FFAR4.
What each result means
C/CTwo copies of the version the research linked to Retinol 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 Retinol levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Retinol levels. This is the starting point the study compared everyone against.
Human molecular genetics · 2011 · PMID 21878437 · open access
Questions about rs10882272
What is rs10882272?
rs10882272 is a single position in the genome, in or near the RBP4 gene. Published research associates it with retinol levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10882272 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 rs10882272 come from?
GWAS Catalog, Human molecular genetics 2011, PMID:21878437. 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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