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Brain age gap derived from white matter

STX6 · rs35306826

What the study found

Who was studied 54,890 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.224 years lower (95% confidence interval 0.18-0.27); p = 1 × 10−25.

How common The A allele had a frequency of about 59% in the people studied.

Where it sits Chromosome 1, band 1q25.3 — in an intron of STX6.

What each result means

A/A Two copies of the version the research linked to Brain age gap derived from white matter. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/T One copy of the version the research linked to Brain age gap derived from white matter. That is a smaller link than two copies.
T/T No copy of the version the research linked to Brain age gap derived from white matter. This is the starting point the study compared everyone against.
Source

Questions about rs35306826

What is rs35306826?

rs35306826 is a single position in the genome, in or near the STX6 gene. Published research associates it with brain age gap derived from white matter. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs35306826 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 rs35306826 come from?

GWAS Catalog, Nature aging 2025, PMID:41044200. 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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Brain age gap derived from white matter (rs35306826). MyGeneLog™. https://www.mygenelog.com/variants/rs35306826

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