Sensitive

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

VMAC · rs146033453

Where this position leads

Condition: Alzheimer's Disease

rs146033453 Condition: Alzheimer's Disease Alzheimer's Disease Condition rs146033453 rs146033453 VMAC

What the study found

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

The effect Each copy of the C 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 = 6 × 10−10.

How common The C allele had a frequency of about 14% in the people studied.

Where it sits Chromosome 19, band 19p13.3 — in an intron of VMAC.

What each result means

C/C 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.
C/T 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.
T/T 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.
Source

Questions about rs146033453

What is rs146033453?

rs146033453 is a single position in the genome, in or near the VMAC 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 rs146033453 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 rs146033453 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 rs146033453 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 (rs146033453). MyGeneLog™. https://www.mygenelog.com/variants/rs146033453

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