Standard

Insomnia

near LINC01392 · rs4730674

Where this position leads

Condition: Insomnia

rs4730674 Condition: Insomnia Insomnia Condition rs4730674 rs4730674 near LINC013…

What the study found

Who was studied 390,751 European ancestry female cases, 1,018,386 European ancestry female controls.

The effect Each copy of the C allele shifted the measure 0.009 lower (95% confidence interval 0.007-0.011); p = 2 × 10−13.

Where it sits Chromosome 7, band 7q31.2 — between genes, 78.4 kb from LINC01392.

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 rs4730674

What is rs4730674?

rs4730674 is a single position in the genome, in or near the near LINC01392 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 rs4730674 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 rs4730674 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 rs4730674 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 (rs4730674). MyGeneLog™. https://www.mygenelog.com/variants/rs4730674

← See all variants