Sensitive

Attention deficit hyperactivity disorder

near DUSP6 · rs12819667

Where this position leads

Condition: ADHD (Attention Deficit Hyperactivity Disorder)

rs12819667 Condition: ADHD (Attention Deficit Hyperactivity Disorder) ADHD (Attention Deficit Hyperactivi… Condition rs12819667 rs12819667 near DUSP6

What the study found

Who was studied 3,323 European ancestry cases, 21,411 European ancestry controls.

The effect Each copy of the T allele carried 0.91 times the odds of Attention deficit hyperactivity disorder (95% confidence interval 0.88-0.94); p = 8 × 10−9.

Where it sits Chromosome 12, band 12q21.33 — between genes, 17.3 kb from DUSP6.

What each result means

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

Questions about rs12819667

What is rs12819667?

rs12819667 is a single position in the genome, in or near the near DUSP6 gene. Published research associates it with attention deficit hyperactivity 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 rs12819667 linked to?

On MyGeneLog this position is linked to ADHD (Attention Deficit Hyperactivity Disorder). The research behind each link, and its sources, are set out on that condition page.

Does having rs12819667 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 rs12819667 come from?

GWAS Catalog, Nature genetics 2024, PMID:38036780. 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.

Attention deficit hyperactivity disorder (rs12819667). MyGeneLog™. https://www.mygenelog.com/variants/rs12819667

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