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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 90,515 individuals.
The effect
Each copy of the C allele shifted the measure 0.576 higher (95% confidence interval 0.4-0.75); p = 3 × 10−10.
Where it sits Chromosome 19, band 19p12 — between genes, 4.9 kb from CPSF6P1.
What each result means
C/CTwo copies of the version the research linked to Sleep (1/3-day periodicity). 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 Sleep (1/3-day periodicity). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Sleep (1/3-day periodicity). This is the starting point the study compared everyone against.
PLoS genetics · 2020 · PMID 33075057 · open access
Questions about rs146923867
What is rs146923867?
rs146923867 is a single position in the genome, in or near the LOC400682 gene. Published research associates it with sleep (1/3-day periodicity). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs146923867 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 rs146923867 come from?
GWAS Catalog, PLoS genetics 2020, PMID:33075057. 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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