Sensitive

Binge eating behaviour in bipolar disorder

PRR5 · rs726170

Where this position leads

Condition: Bipolar Disorder

rs726170 Condition: Bipolar Disorder Bipolar Disorder Condition rs726170 rs726170 PRR5

What the study found

Who was studied 398 European ancestry bipolar disorder cases, 1,231 European ancestry bipolar disorder controls.

The effect Each copy of the T allele carried 1.92 times the odds of Binge eating behaviour in bipolar disorder; p = 3 × 10−8.

How common The T allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 22, band 22q13.31 — in an intron of ARHGAP8.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Binge eating behaviour in bipolar disorder — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Binge eating behaviour in bipolar disorder.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Binge eating behaviour in bipolar disorder compared to the general population.
Source

Questions about rs726170

What is rs726170?

rs726170 is a single position in the genome, in or near the PRR5 gene. Published research associates it with binge eating behaviour in bipolar 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 rs726170 linked to?

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

Does having rs726170 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 rs726170 come from?

GWAS Catalog, Transl Psychiatry 2018, PMID:29391396. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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