Sensitive

Depression

LINC02882 · rs17828731

Where this position leads

Condition: Endometriosis and Depression: Shared Genetics

rs17828731 Condition: Endometriosis and Depression: Shared Genetics Endometriosis and Depression: Share… Condition rs17828731 rs17828731 LINC02882

What the study found

Who was studied 688,809 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 5.67 z score higher; p = 1 × 10−8.

Where it sits Chromosome 12, band 12q21.1 — in an intron of LINC02882.

What each result means

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

Questions about rs17828731

What is rs17828731?

rs17828731 is a single position in the genome, in or near the LINC02882 gene. Published research associates it with depression. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs17828731 linked to?

On MyGeneLog this position is linked to Endometriosis and Depression: Shared Genetics. The research behind each link, and its sources, are set out on that condition page.

Does having rs17828731 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 rs17828731 come from?

GWAS Catalog, Nature genetics 2018, PMID:29942085. 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.

Depression (rs17828731). MyGeneLog™. https://www.mygenelog.com/variants/rs17828731

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