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Who was studied 38,000 South Asian ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.127 lower (95% confidence interval 0.11-0.14); p = 4 × 10−72.
Where it sits Chromosome 8, band 8q24.21 — inside CCDC26.
What each result means
A/ANo copy of the version the research linked to Monocyte count. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Monocyte count. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Monocyte count. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2024 · PMID 39414775 · open access
Questions about rs10103048
What is rs10103048?
rs10103048 is a single position in the genome, in or near the CCDC26 gene. Published research associates it with monocyte count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs10103048 linked to?
On MyGeneLog this position is linked to Monocyte Count, Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.
Does having rs10103048 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 rs10103048 come from?
GWAS Catalog, Nature communications 2024, PMID:39414775. 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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