LINC02210-CRHR1 · rs17689471
Where this position leads
Condition: Major Depressive Disorder
What the study found
Who was studied 65,075 European ancestry MDD cases, 24,274 European ancestry hospitalized COVID-19 cases, 2,294,081 European ancestry controls.
The effect The reported allele is C; the catalogue records no effect size ; p = 1 × 10−12.
Where it sits Chromosome 17, band 17q21.31 — in an intron of LINC02210-CRHR1.
rs17689471 is a single position in the genome, in or near the LINC02210-CRHR1 gene. Published research associates it with major depressive disorder or hospitalized covid-19 (pleiotropy). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Major Depressive Disorder. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, Frontiers in psychiatry 2023, PMID:37426090. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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.
Major depressive disorder or hospitalized COVID-19 (pleiotropy) (rs17689471). MyGeneLog™. https://www.mygenelog.com/variants/rs17689471