White matter microstructure (axial diusivities) Anterior corona radiata (PC2)
near ZNF275 · rs184885934
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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 37,772 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 6.24 z score lower; p = 5 × 10−10.
Where it sits Chromosome X, band Xq28 — between genes, 8.9 kb from ZNF275.
What each result means
C/CNo copy of the version the research linked to White matter microstructure (axial diusivities) Anterior corona radiata (PC2). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to White matter microstructure (axial diusivities) Anterior corona radiata (PC2). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to White matter microstructure (axial diusivities) Anterior corona radiata (PC2). That is the strongest link of the three results. A link in a study is not a diagnosis.
Science advances · 2025 · PMID 39854466 · open access
Questions about rs184885934
What is rs184885934?
rs184885934 is a single position in the genome, in or near the near ZNF275 gene. Published research associates it with white matter microstructure (axial diusivities) anterior corona radiata (pc2). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs184885934 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 rs184885934 come from?
GWAS Catalog, Science advances 2025, PMID:39854466. 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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