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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 121,745 Japanese ancestry individuals; replicated in at least 101,293 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.039 lower (95% confidence interval 0.029-0.049); p = 7 × 10−14.
How common The A allele had a frequency of about 81% in the people studied.
Where it sits Chromosome 2, band 2q31.1 — in an intron of LRP2.
What each result means
A/ATwo copies of the version the research linked to Serum uric acid levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Serum uric acid levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Serum uric acid levels. This is the starting point the study compared everyone against.
Communications biology · 2019 · PMID 30993211 · open access
Questions about rs16856823
What is rs16856823?
rs16856823 is a single position in the genome, in or near the LRP2 gene. Published research associates it with serum uric acid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs16856823 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 rs16856823 come from?
GWAS Catalog, Communications biology 2019, PMID:30993211. 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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