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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 35,269 European ancestry cases, 63,451 European ancestry controls.
The effect
Each copy of the T allele carried 1.08 times the odds of Trauma exposure (95% confidence interval 1.05-1.11); p = 1 × 10−8.
How common The T allele had a frequency of about 37% in the people studied.
Where it sits Chromosome 14, band 14q32.2 — between genes, 47.4 kb from LINC02295.
What each result means
A/ANo copy of the version the research linked to Trauma exposure. This is the starting point the study compared everyone against.
A/TOne copy of the version the research linked to Trauma exposure. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Trauma exposure. That is the strongest link of the three results. A link in a study is not a diagnosis.
Molecular psychiatry · 2020 · PMID 31969693 · open access
Questions about rs28740872
What is rs28740872?
rs28740872 is a single position in the genome, in or near the near LINC02295 gene. Published research associates it with trauma exposure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs28740872 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 rs28740872 come from?
GWAS Catalog, Molecular psychiatry 2020, PMID:31969693. 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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