Standard

Insomnia

near ZNF646P1 · rs4883690

Where this position leads

Condition: Insomnia

rs4883690 Condition: Insomnia Insomnia Condition rs4883690 rs4883690 near ZNF646P1

What the study found

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 0.014 higher (95% confidence interval 0.012-0.016); p = 4 × 10−28.

Where it sits Chromosome 13, band 13q14.3 — between genes, 35.1 kb from ZNF646P1.

What each result means

C/C 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.
C/G One copy of the version the research linked to Insomnia. That is a smaller link than two copies.
G/G No copy of the version the research linked to Insomnia. This is the starting point the study compared everyone against.
Source

Questions about rs4883690

What is rs4883690?

rs4883690 is a single position in the genome, in or near the near ZNF646P1 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 rs4883690 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 rs4883690 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 rs4883690 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 (rs4883690). MyGeneLog™. https://www.mygenelog.com/variants/rs4883690

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