Other CNS infection and poliomyelitis (PheCode 324)
near CDRT15P3 · rs186305933
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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 263 African American or Afro-Caribbean cases, 121,441 African American or Afro-Caribbean controls, 1,042 European ancestry cases, 449,511 European ancestry controls.
The effect
Each copy of the G allele shifted the measure 3.18 lower (95% confidence interval 3.15-3.2); p = 4 × 10−11.
How common The G allele had a frequency of about 100% in the people studied.
Where it sits Chromosome 2, band 2q21.2 — between genes, 68.4 kb from CDRT15P3.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of Other CNS infection and poliomyelitis (PheCode 324) — no copies of the reported risk allele.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Other CNS infection and poliomyelitis (PheCode 324).
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Other CNS infection and poliomyelitis (PheCode 324) compared to the general population.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs186305933
What is rs186305933?
rs186305933 is a single position in the genome, in or near the near CDRT15P3 gene. Published research associates it with other cns infection and poliomyelitis (phecode 324). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs186305933 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 rs186305933 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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Other CNS infection and poliomyelitis (PheCode 324) (rs186305933). MyGeneLog™. https://www.mygenelog.com/variants/rs186305933