Benign neoplasm of bone and articular cartilage (PheCode 213)
ARRDC3-AS1 · rs185990766
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What the study found
Who was studied 268 African American or Afro-Caribbean cases, 120,957 African American or Afro-Caribbean controls, 717 European ancestry cases, 448,500 European ancestry controls.
The effect
Each copy of the C allele shifted the measure 4.39 lower (95% confidence interval 4.38-4.4); p = 1 × 10−12.
How common The C allele had a frequency of about 100% in the people studied.
Where it sits Chromosome 5, band 5q14.3 — in an intron of ARRDC3-AS1.
What each result means
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Benign neoplasm of bone and articular cartilage (PheCode 213) compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Benign neoplasm of bone and articular cartilage (PheCode 213).
T/TPublished research associates this genotype with typical/baseline likelihood of Benign neoplasm of bone and articular cartilage (PheCode 213) — no copies of the reported risk allele.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs185990766
What is rs185990766?
rs185990766 is a single position in the genome, in or near the ARRDC3-AS1 gene. Published research associates it with benign neoplasm of bone and articular cartilage (phecode 213). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs185990766 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 rs185990766 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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Benign neoplasm of bone and articular cartilage (PheCode 213) (rs185990766). MyGeneLog™. https://www.mygenelog.com/variants/rs185990766