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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 T allele shifted the measure 2.3 higher (95% confidence interval 1.54-3.06); p = 3 × 10−9.
Where it sits Chromosome 1, band 1q25.3 — in an intron of LAMC1.
What each result means
C/CNo copy of the version the research linked to Accessory basal nucleus volume. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Accessory basal nucleus volume. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Accessory basal 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 rs116472807
What is rs116472807?
rs116472807 is a single position in the genome, in or near the LAMC1 gene. Published research associates it with accessory basal 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 rs116472807 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 rs116472807 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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