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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 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 1.83 lower (95% confidence interval 1.33-2.32); p = 2 × 10−12.
Where it sits Chromosome 11, band 11q24.2 — between genes, 14.2 kb from NRGN.
What each result means
A/ATwo copies of the version the research linked to VSIG2 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to VSIG2 protein levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to VSIG2 protein levels. This is the starting point the study compared everyone against.
Scientific reports · 2024 · PMID 38565889 · open access
Questions about rs369634369
What is rs369634369?
rs369634369 is a single position in the genome, in or near the near NRGN gene. Published research associates it with vsig2 protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs369634369 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 rs369634369 come from?
GWAS Catalog, Scientific reports 2024, PMID:38565889. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
VSIG2 protein levels (rs369634369). MyGeneLog™. https://www.mygenelog.com/variants/rs369634369