Sensitive

Alzheimer's disease

MRC1 · rs4748424

Where this position leads

Condition: Alzheimer's Disease Risk (APOE)

rs4748424 Condition: Alzheimer's Disease Risk (APOE) Alzheimer's Disease Risk (APOE) Condition rs4748424 rs4748424 MRC1

What the study found

Who was studied 5,705 European ancestry cases, 7,067 European ancestry controls.

The effect Each copy of the G allele carried 0.68 times the odds of Alzheimer's disease (95% confidence interval 0.601-0.774); p = 3 × 10−9.

How common The G allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 10, band 10p12.33 — in an intron of MRC1.

What each result means

A/A No copy of the version the research linked to 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. That is a smaller link than two copies.
G/G Two 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.
Source

Questions about rs4748424

What is rs4748424?

rs4748424 is a single position in the genome, in or near the MRC1 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 rs4748424 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 rs4748424 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 rs4748424 come from?

GWAS Catalog, Frontiers in aging neuroscience 2021, PMID:34122051. 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 (rs4748424). MyGeneLog™. https://www.mygenelog.com/variants/rs4748424

← See all variants