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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 154,355 East Asian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0242 higher (95% confidence interval 0.017-0.031); p = 2 × 10−11.
How common The G allele had a frequency of about 34% in the people studied.
Where it sits Chromosome 10, band 10q25.2 — between genes, 20.5 kb from MXI1.
What each result means
A/ANo copy of the version the research linked to White blood cell count. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to White blood cell count. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to White blood cell count. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs79404554 is a single position in the genome, in or near the near MXI1 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.
Does having rs79404554 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 rs79404554 come from?
GWAS Catalog, Nature genetics 2021, PMID:34594039. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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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.
White blood cell count (rs79404554). MyGeneLog™. https://www.mygenelog.com/variants/rs79404554