white blood cell count (WBC, mean, inv-norm transformed)
DBN1 · rs371071053
0 112216Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others6Total11Counted 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.
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 108,896 African American or Afro-Caribbean individuals.
The effect
Each copy of the C allele shifted the measure 0.421 lower (95% confidence interval 0.35-0.49); p = 5 × 10−32.
How common The C allele had a frequency of about 99% in the people studied.
Where it sits Chromosome 5, band 5q35.3 — in the 5′ untranslated region of DBN1.
What each result means
C/CTwo copies of the version the research linked to white blood cell count (WBC, mean, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to white blood cell count (WBC, mean, inv-norm transformed). That is a smaller link than two copies.
T/TNo copy of the version the research linked to white blood cell count (WBC, mean, inv-norm transformed). This is the starting point the study compared everyone against.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs371071053
What is rs371071053?
rs371071053 is a single position in the genome, in or near the DBN1 gene. Published research associates it with white blood cell count (wbc, mean, 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 rs371071053 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 rs371071053 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 112216Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others6Total11Counted 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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