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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 2,893 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.209 higher (95% confidence interval 0.16-0.26); p = 2 × 10−17.
How common The T allele had a frequency of about 47% in the people studied.
Where it sits Chromosome 4, band 4q22.3 — between genes, 42.5 kb from RPL30P6.
What each result means
C/CNo copy of the version the research linked to Netrin receptor UNC5C levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Netrin receptor UNC5C levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Netrin receptor UNC5C levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2021 · PMID 34857772 · open access
Questions about rs36111522
What is rs36111522?
rs36111522 is a single position in the genome, in or near the near RPL30P6 gene. Published research associates it with netrin receptor unc5c levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs36111522 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 rs36111522 come from?
GWAS Catalog, Nature communications 2021, PMID:34857772. 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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