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Who was studied 2,559 Hispanic cases, 5,908 Hispanic controls.
The effect
Each copy of the C allele carried 9.67 times the odds of Alzheimer's disease (95% confidence interval 4.71-19.88); p = 7 × 10−10.
How common The C allele had a frequency of about 0% in the people studied.
Where it sits Chromosome 14, band 14q24.2 — in an intron of ZFYVE1.
What each result means
C/CTwo copies of the version the research linked to Alzheimer's disease. 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 Alzheimer's disease. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Alzheimer's disease. This is the starting point the study compared everyone against.
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026 · PMID 41755704 · open access
Questions about rs182804071
What is rs182804071?
rs182804071 is a single position in the genome, in or near the ZFYVE1 gene. Published research associates it with alzheimer's disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs182804071 linked to?
On MyGeneLog this position is linked to Alzheimer's Disease Risk (APOE). The research behind each link, and its sources, are set out on that condition page.
Does having rs182804071 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 rs182804071 come from?
GWAS Catalog, Alzheimer's & dementia : the journal of the Alzheimer's Association 2026, PMID:41755704. 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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