CNOT9 · rs589967
Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 52,141 European ancestry females; replicated in 89,584 European ancestry females.
The effect Each copy of the T allele shifted the measure 0.0214 lower; p = 1 × 10−10.
How common The T allele had a frequency of about 43% in the people studied.
Where it sits Chromosome 2, band 2q35 — in an intron of CNOT9.
rs589967 is a single position in the genome, in or near the CNOT9 gene. Published research associates it with hemoglobin concentration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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, The Journal of nutritional biochemistry 2023, PMID:35964923. 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.
Hemoglobin concentration (rs589967). MyGeneLog™. https://www.mygenelog.com/variants/rs589967