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Who was studied 222,753 European ancestry male cases, 993,280 European ancestry male controls.
The effect
Each copy of the C allele shifted the measure 0.011 higher (95% confidence interval 0.0071-0.0149); p = 4 × 10−11.
Where it sits Chromosome 20, band 20q13.2 — in an intron of LINC01524.
What each result means
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Insomnia compared to the general population.
C/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Insomnia.
G/GPublished research associates this genotype with typical/baseline likelihood of Insomnia — no copies of the reported risk allele.
rs13043844 is a single position in the genome, in or near the LINC01524 gene. Published research associates it with insomnia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs13043844 linked to?
On MyGeneLog this position is linked to Insomnia. The research behind each link, and its sources, are set out on that condition page.
Does having rs13043844 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 rs13043844 come from?
GWAS Catalog, Nature genetics 2022, PMID:35835914. 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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