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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 31,690 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.4 higher (95% confidence interval 0.28-0.52); p = 4 × 10−11.
Where it sits Chromosome 4, band 4q12 — in an intron of PDCL2.
What each result means
A/ANo copy of the version the research linked to Medial nucleus volume. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Medial nucleus volume. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Medial nucleus volume. That is the strongest link of the three results. A link in a study is not a diagnosis.
Biological psychiatry · 2024 · PMID 37391117 · open access
Questions about rs11133400
What is rs11133400?
rs11133400 is a single position in the genome, in or near the PDCL2 gene. Published research associates it with medial nucleus volume. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11133400 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 rs11133400 come from?
GWAS Catalog, Biological psychiatry 2024, PMID:37391117. 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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