Sensitive

Alzheimer's disease, proxy Alzheimer's disease or related dementias

CYP20A1 · rs115600411

Where this position leads

Condition: Alzheimer's Disease

rs115600411 Condition: Alzheimer's Disease Alzheimer's Disease Condition rs115600411 rs115600411 CYP20A1

What the study found

Who was studied 128,681 European ancestry cases, 849,833 European ancestry controls.

The effect Each copy of the G allele carried 0.95 times the odds of Alzheimer's disease, proxy Alzheimer's disease or related dementias (95% confidence interval 0.93-0.96); p = 2 × 10−9.

How common The G allele had a frequency of about 13% in the people studied.

Where it sits Chromosome 2, band 2q33.2 — in an intron of CYP20A1.

What each result means

C/C No copy of the version the research linked to Alzheimer's disease, proxy Alzheimer's disease or related dementias. This is the starting point the study compared everyone against.
C/G One copy of the version the research linked to Alzheimer's disease, proxy Alzheimer's disease or related dementias. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Alzheimer's disease, proxy Alzheimer's disease or related dementias. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs115600411

What is rs115600411?

rs115600411 is a single position in the genome, in or near the CYP20A1 gene. Published research associates it with alzheimer's disease, proxy alzheimer's disease or related dementias. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs115600411 linked to?

On MyGeneLog this position is linked to Alzheimer's Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs115600411 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 rs115600411 come from?

GWAS Catalog, Nature genetics 2026, PMID:42237039. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Alzheimer's disease, proxy Alzheimer's disease or related dementias (rs115600411). MyGeneLog™. https://www.mygenelog.com/variants/rs115600411

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