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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 497,803 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0344 higher (95% confidence interval 0.022-0.046); p = 2 × 10−8.
Where it sits Chromosome 2, band 2p16.1 — in an intron of VRK2.
What each result means
A/ATwo copies of the version the research linked to Post-traumatic stress disorder (phenotype risk score). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Post-traumatic stress disorder (phenotype risk score). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Post-traumatic stress disorder (phenotype risk score). This is the starting point the study compared everyone against.
Molecular psychiatry · 2022 · PMID 35181757 · open access
Questions about rs77736916
What is rs77736916?
rs77736916 is a single position in the genome, in or near the VRK2 gene. Published research associates it with post-traumatic stress disorder (phenotype risk score). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs77736916 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 rs77736916 come from?
GWAS Catalog, Molecular psychiatry 2022, PMID:35181757. 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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