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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 19,099 European ancestry attention deficit hyperactivity disorder cases, 18,381 European ancestry autism spectrum disorder cases, 20,352 European ancestry bipolar disorder cases, 170,756 European ancestry major depressive disorder cases, 33,640 European ancestry schizophrenia cases, 466,420 European ancestry controls.
The effect
Each copy of the C allele shifted the measure 8.91 z score higher; p = 5 × 10−19.
Where it sits Chromosome 6, band 6p22.1 — in the 3′ untranslated region of ZSCAN12.
What each result means
C/CTwo copies of the version the research linked to Neuropsychiatric disorders. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Neuropsychiatric disorders. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Neuropsychiatric disorders. This is the starting point the study compared everyone against.
Translational psychiatry · 2021 · PMID 33479212 · open access
Questions about rs67981811
What is rs67981811?
rs67981811 is a single position in the genome, in or near the ZSCAN12 gene. Published research associates it with neuropsychiatric disorders. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs67981811 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 rs67981811 come from?
GWAS Catalog, Translational psychiatry 2021, PMID:33479212. 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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