Standard

Insomnia

near LINC01812 · rs13032405

Where this position leads

Condition: Insomnia

rs13032405 Condition: Insomnia Insomnia Condition rs13032405 rs13032405 near LINC018…

What the study found

Who was studied 593,724 European ancestry cases, 1,771,286 European ancestry controls.

The effect Each copy of the T allele shifted the measure 0.006 higher (95% confidence interval 0.004-0.008); p = 4 × 10−11.

Where it sits Chromosome 2, band 2p14 — between genes, 48.9 kb from LINC01812.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Insomnia — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Insomnia.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Insomnia compared to the general population.
Source

Questions about rs13032405

What is rs13032405?

rs13032405 is a single position in the genome, in or near the near LINC01812 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 rs13032405 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 rs13032405 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 rs13032405 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.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Insomnia (rs13032405). MyGeneLog™. https://www.mygenelog.com/variants/rs13032405

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