NTF3 · rs7138947
Where this position leads
Condition: Insomnia
What the study found
Who was studied 2,297 European American cases, 334 African American cases, 606 Latino American cases, 9,176 European American controls, 2,345 African American controls, 2,893 Latino American controls.
The effect Each copy of the A allele carried 3.15 times the odds of Insomnia (95% confidence interval -); p = 2 × 10−8.
Where it sits Chromosome 12, band 12p13.31 — inside NTF3.
rs7138947 is a single position in the genome, in or near the NTF3 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. 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, Mol Psychiatry 2018, PMID:29520036. 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 (rs7138947). MyGeneLog™. https://www.mygenelog.com/variants/rs7138947