white blood cell count (WBC, minimum, inv-norm transformed)
CNIH3 · rs10799574
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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 108,942 African American or Afro-Caribbean individuals, 49,991 Hispanic or Latin American individuals, 5,838 East Asian ancestry individuals, 381,267 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0305 higher (95% confidence interval 0.024-0.037); p = 8 × 10−21.
How common The T allele had a frequency of about 41% in the people studied.
Where it sits Chromosome 1, band 1q42.12 — inside CNIH3.
What each result means
G/GNo copy of the version the research linked to white blood cell count (WBC, minimum, inv-norm transformed). This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to white blood cell count (WBC, minimum, inv-norm transformed). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to white blood cell count (WBC, minimum, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs10799574
What is rs10799574?
rs10799574 is a single position in the genome, in or near the CNIH3 gene. Published research associates it with white blood cell count (wbc, minimum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10799574 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 rs10799574 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 1412317Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others7Total14Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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