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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 474,001 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.015 SD unit lower (95% confidence interval 0.011-0.019); p = 2 × 10−11.
How common The T allele had a frequency of about 30% in the people studied.
Where it sits Chromosome 16, band 16q21 — in an intron of CCDC102A.
What each result means
G/GNo copy of the version the research linked to Basophil count. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Basophil count. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Basophil count. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs9928015 is a single position in the genome, in or near the CCDC102A gene. Published research associates it with basophil count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9928015 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 rs9928015 come from?
GWAS Catalog, Cell 2020, PMID:32888493. 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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