Sensitive

Anxiety disorder

DCC · rs17408393

Where this position leads

Condition: Anxiety Disorder

rs17408393 Condition: Anxiety Disorder Anxiety Disorder Condition rs17408393 rs17408393 DCC

What the study found

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

The effect Each copy of the A allele shifted the measure 0.0139 lower; p = 3 × 10−11.

Where it sits Chromosome 18, band 18q21.2 — in an intron of DCC.

What each result means

A/A 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.
A/G One copy of the version the research linked to Anxiety disorder. That is a smaller link than two copies.
G/G No copy of the version the research linked to Anxiety disorder. This is the starting point the study compared everyone against.
Source

Questions about rs17408393

What is rs17408393?

rs17408393 is a single position in the genome, in or near the DCC 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 rs17408393 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 rs17408393 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 rs17408393 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 (rs17408393). MyGeneLog™. https://www.mygenelog.com/variants/rs17408393

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