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Cerebrospinal fluid soluble TREM2 levels

MS4A6E · rs11827324

What the study found

Who was studied 3,350 European ancestry individuals, 250 non-European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.336 higher (95% confidence interval 0.29-0.38); p = 7 × 10−52.

How common The G allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 11, band 11q12.2 — in an intron of MS4A6E.

What each result means

A/A No copy of the version the research linked to Cerebrospinal fluid soluble TREM2 levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Cerebrospinal fluid soluble TREM2 levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Cerebrospinal fluid soluble TREM2 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs11827324

What is rs11827324?

rs11827324 is a single position in the genome, in or near the MS4A6E gene. Published research associates it with cerebrospinal fluid soluble trem2 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11827324 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 rs11827324 come from?

GWAS Catalog, Molecular neurodegeneration 2024, PMID:38172904. 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.

Cerebrospinal fluid soluble TREM2 levels (rs11827324). MyGeneLog™. https://www.mygenelog.com/variants/rs11827324

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