Sensitive

Anxiety disorder

YLPM1 · rs10138360

Where this position leads

Condition: Anxiety Disorder

rs10138360 Condition: Anxiety Disorder Anxiety Disorder Condition rs10138360 rs10138360 YLPM1

What the study found

Who was studied 1,096,458 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0113 lower; p = 3 × 10−8.

Where it sits Chromosome 14, band 14q24.3 — in an intron of YLPM1.

What each result means

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

Questions about rs10138360

What is rs10138360?

rs10138360 is a single position in the genome, in or near the YLPM1 gene. Published research associates it with anxiety disorder. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs10138360 linked to?

On MyGeneLog this position is linked to Anxiety Disorder. The research behind each link, and its sources, are set out on that condition page.

Does having rs10138360 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 rs10138360 come from?

GWAS Catalog, Nature genetics 2024, PMID:39294497. 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.

Anxiety disorder (rs10138360). MyGeneLog™. https://www.mygenelog.com/variants/rs10138360

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