Standard

Insomnia

near RNU6-367P · rs75619216

Where this position leads

Condition: Insomnia

rs75619216 Condition: Insomnia Insomnia Condition rs75619216 rs75619216 near RNU6-36…

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 0.012 lower (95% confidence interval 0.0081-0.0159); p = 1 × 10−8.

Where it sits Chromosome 3, band 3p21.33 — between genes, 158.1 kb from RNU6-367P.

What each result means

C/C No copy of the version the research linked to Insomnia. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Insomnia. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Insomnia. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs75619216

What is rs75619216?

rs75619216 is a single position in the genome, in or near the near RNU6-367P 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 rs75619216 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 rs75619216 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 rs75619216 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 (rs75619216). MyGeneLog™. https://www.mygenelog.com/variants/rs75619216

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