PLXNA2 · rs192568756
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 809 African American or Afro-Caribbean cases, 119,135 African American or Afro-Caribbean controls, 3,141 European ancestry cases, 442,954 European ancestry controls, 524 Hispanic or Latin American cases, 58,556 Hispanic or Latin American controls.
The effect Each copy of the A allele shifted the measure 2.47 lower (95% confidence interval 2.43-2.51); p = 1 × 10−12.
How common The A allele had a frequency of about 100% in the people studied.
Where it sits Chromosome 1, band 1q32.2 — in an intron of PLXNA2.
rs192568756 is a single position in the genome, in or near the PLXNA2 gene. Published research associates it with other disorders of cervical region (phecode 723). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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.
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.
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.
Other disorders of cervical region (PheCode 723) (rs192568756). MyGeneLog™. https://www.mygenelog.com/variants/rs192568756