HEXIM1 · rs9894577
Where this position leads
Conditions: Insomnia, Osteoarthritis
What the study found
Who was studied 404,588 European ancestry individuals, 17,651 European, Hispanic and African ancestry individuals.
The effect The reported allele is A; the catalogue records no effect size ; p = 1 × 10−10.
How common The A allele had a frequency of about 35% in the people studied.
Where it sits Chromosome 17, band 17q21.31 — between genes, 1.7 kb from ACBD4.
rs9894577 is a single position in the genome, in or near the HEXIM1 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.
On MyGeneLog this position is linked to Insomnia, Osteoarthritis. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, Scientific reports 2020, PMID:32332799. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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 (rs9894577). MyGeneLog™. https://www.mygenelog.com/variants/rs9894577