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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 34,794 British ancestry individuals.
The effect
The reported allele is C; the catalogue records no effect size
; p = 9 × 10−10.
Where it sits Chromosome 11, band 11q21 — in an intron of LNCRNA-IUR.
What each result means
A/ANo copy of the version the research linked to Basal ganglia structure. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Basal ganglia structure. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Basal ganglia structure. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2024 · PMID 39353893 · open access
Questions about rs3214031
What is rs3214031?
rs3214031 is a single position in the genome, in or near the LNCRNA-IUR gene. Published research associates it with basal ganglia structure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs3214031 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 rs3214031 come from?
GWAS Catalog, Nature communications 2024, PMID:39353893. 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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