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Basal ganglia structure

TESHL · rs56000151

What the study found

Who was studied 34,794 British ancestry individuals.

The effect The reported allele is G; the catalogue records no effect size ; p = 1 × 10−8.

Where it sits Chromosome 2, band 2q35 — in an intron of TESHL.

What each result means

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

Questions about rs56000151

What is rs56000151?

rs56000151 is a single position in the genome, in or near the TESHL gene. Published research associates it with basal ganglia structure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs56000151 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 rs56000151 come from?

GWAS Catalog, Nature communications 2024, PMID:39353893. 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.

Basal ganglia structure (rs56000151). MyGeneLog™. https://www.mygenelog.com/variants/rs56000151

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