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Cerebrospinal fluid protein ADAM15 levels

MEX3A · rs3738593

What the study found

Who was studied 2,524 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.185 lower (95% confidence interval 0.14-0.23); p = 2 × 10−16.

How common The T allele had a frequency of about 22% in the people studied.

Where it sits Chromosome 1, band 1q22 — in the 3′ untranslated region of MEX3A.

What each result means

C/C No copy of the version the research linked to Cerebrospinal fluid protein ADAM15 levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Cerebrospinal fluid protein ADAM15 levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Cerebrospinal fluid protein ADAM15 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs3738593

What is rs3738593?

rs3738593 is a single position in the genome, in or near the MEX3A gene. Published research associates it with cerebrospinal fluid protein adam15 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3738593 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 rs3738593 come from?

GWAS Catalog, Science translational medicine 2026, PMID:42054495. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Cerebrospinal fluid protein ADAM15 levels (rs3738593). MyGeneLog™. https://www.mygenelog.com/variants/rs3738593

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