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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 106,192 European ancestry cases, 305,742 European ancestry controls; replicated in 47,180 adults, 10,554 children or adolescents.
The effect
The reported allele is C; the catalogue records no effect size
; p = 3 × 10−18.
Where it sits Chromosome 2, band 2q14.1 — in an intron of LINC02966.
What each result means
A/ANo copy of the version the research linked to Sleep duration (short sleep). This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Sleep duration (short sleep). That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Sleep duration (short sleep). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2019 · PMID 30846698 · open access
Questions about rs2863957
What is rs2863957?
rs2863957 is a single position in the genome, in or near the PAX8 gene. Published research associates it with sleep duration (short sleep). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2863957 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 rs2863957 come from?
GWAS Catalog, Nat Commun 2019, PMID:30846698. 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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