Standard

Insomnia

near LYPLA2P1 · rs118109745

Where this position leads

Condition: Insomnia

rs118109745 Condition: Insomnia Insomnia Condition rs118109745 rs118109745 near LYPLA2P1

What the study found

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

The effect Each copy of the A allele shifted the measure 0.026 lower (95% confidence interval 0.018-0.034); p = 4 × 10−10.

Where it sits Chromosome 6, band 6p21.32 — between genes, 11.6 kb from LYPLA2P1.

What each result means

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

Questions about rs118109745

What is rs118109745?

rs118109745 is a single position in the genome, in or near the near LYPLA2P1 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 rs118109745 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 rs118109745 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 rs118109745 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 (rs118109745). MyGeneLog™. https://www.mygenelog.com/variants/rs118109745

← See all variants