CSF3 · rs4065321
Where this position leads
Condition: Blood Cell Counts
What the study found
Who was studied 14,677 Japanese ancestry individuals.
The effect Each copy of the T allele shifted the measure 0.094 lower (95% confidence interval 0.070-0.118); p = 3 × 10−14.
How common The T allele had a frequency of about 32% in the people studied.
Where it sits Chromosome 17, band 17q21.1 — in an intron of PSMD3.
What people read about alongside this
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
rs4065321 is a single position in the genome, in or near the CSF3 gene. Published research associates it with white blood cell count. 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 Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
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, Nat Genet 2010, PMID:20139978. 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.
White blood cell count (rs4065321). MyGeneLog™. https://www.mygenelog.com/variants/rs4065321