Sensitive

Alzheimer's disease or family history of Alzheimer's disease

CD2AP · rs10948363

Where this position leads

Condition: Alzheimer's Disease

rs10948363 Condition: Alzheimer's Disease Alzheimer's Disease Condition rs10948363 rs10948363 CD2AP

What the study found

Who was studied 24,087 European ancestry late-onset Alzheimer's disease cases, 47,793 European ancestry individuals with family history of Alzheimer's disease, 383,378 European ancestry controls.

The effect Each copy of the G allele shifted the measure 5.72 z-unit higher; p = 1 × 10−8.

How common The G allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 6, band 6p12.3 — in an intron of CD2AP.

What each result means

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

Questions about rs10948363

What is rs10948363?

rs10948363 is a single position in the genome, in or near the CD2AP gene. Published research associates it with alzheimer's disease or family history of 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 rs10948363 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 rs10948363 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 rs10948363 come from?

GWAS Catalog, Nature genetics 2019, PMID:30617256. 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 or family history of Alzheimer's disease (rs10948363). MyGeneLog™. https://www.mygenelog.com/variants/rs10948363

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