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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 115 Asian ancestry cases, 4,082 Asian ancestry controls.
The effect
Each copy of the T allele carried 3.07 times the odds of Suicide attempts (95% confidence interval 2.68-3.46); p = 3 × 10−8.
Where it sits Chromosome 15, band 15q21.1 — in an intron of FBN1.
What each result means
C/CNo copy of the version the research linked to Suicide attempts. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Suicide attempts. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Suicide attempts. That is the strongest link of the three results. A link in a study is not a diagnosis.
Molecular psychiatry · 2022 · PMID 35347246 · open access
Questions about rs57790277
What is rs57790277?
rs57790277 is a single position in the genome, in or near the FBN1 gene. Published research associates it with suicide attempts. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs57790277 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 rs57790277 come from?
GWAS Catalog, Molecular psychiatry 2022, PMID:35347246. 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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