Sensitive

Attention deficit hyperactivity disorder

SGO1-AS1 · rs56135409

Where this position leads

Condition: ADHD (Attention Deficit Hyperactivity Disorder)

rs56135409 Condition: ADHD (Attention Deficit Hyperactivity Disorder) ADHD (Attention Deficit Hyperactivi… Condition rs56135409 rs56135409 SGO1-AS1

What the study found

Who was studied 19,099 European ancestry cases, 72 non-European ancestry cases, 1,012 Han Chinese ancestry cases, 34,194 European ancestry controls, 72 non-European ancestry controls, 925 Han Chinese ancestry controls; replicated in 5,085 Icelandic ancestry cases, 5,857 cases, 131,122 Icelandic ancestry controls, 70,393 controls.

The effect The reported allele is C; the catalogue records no effect size ; p = 5 × 10−8.

Where it sits Chromosome 3, band 3p24.3 — in an intron of SGO1-AS1.

What each result means

A/A No copy of the version the research linked to Attention deficit hyperactivity disorder. This is the starting point the study compared everyone against.
A/C One copy of the version the research linked to Attention deficit hyperactivity disorder. That is a smaller link than two copies.
C/C 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 rs56135409

What is rs56135409?

rs56135409 is a single position in the genome, in or near the SGO1-AS1 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 rs56135409 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 rs56135409 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 rs56135409 come from?

GWAS Catalog, Nature genetics 2019, PMID:30478444. 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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Attention deficit hyperactivity disorder (rs56135409). MyGeneLog™. https://www.mygenelog.com/variants/rs56135409

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