near HSPE1P1 · rs6028719
Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 223 French ancestry female cases, 1,204 French ancestry female controls.
The effect Each copy of the T allele carried 1.85 times the odds of Late-onset postpartum depression (95% confidence interval 1.49-2.3); p = 2 × 10−8.
Where it sits Chromosome 20, band 20q12 — between genes, 12.5 kb from HSPE1P1.
rs6028719 is a single position in the genome, in or near the near HSPE1P1 gene. Published research associates it with late-onset postpartum depression. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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, European psychiatry : the journal of the Association of European Psychiatrists 2024, PMID:38555957. 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.
Late-onset postpartum depression (rs6028719). MyGeneLog™. https://www.mygenelog.com/variants/rs6028719