near PDCL3P4 · rs11919389
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 2,544 African ancestry cases, 31,176 African ancestry controls, 700 Middle Eastern ancestry cases, 13,360 Middle Eastern ancestry controls, 1,495 East Asian ancestry cases, 15,499 East Asian ancestry controls, 38,984 European ancestry cases, 1,644,784 European ancestry controls, 1,688 South Asian ancestry cases, 42,016 South Asian ancestry controls, 4,151 Hispanic or Latin American cases, 23,371 Hispanic or Latin American controls.
The effect Each copy of the C allele carried 0.94 times the odds of SARS-CoV-2 infection (95% confidence interval 0.9273018223094552-0.9556267949509863); p = 3 × 10−15.
How common The C allele had a frequency of about 35% in the people studied.
Where it sits Chromosome 3, band 3q12.3 — between genes, 6.9 kb from PDCL3P4.
rs11919389 is a single position in the genome, in or near the near PDCL3P4 gene. Published research associates it with sars-cov-2 infection. 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, Nature 2021, PMID:34237774. 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.
SARS-CoV-2 infection (rs11919389). MyGeneLog™. https://www.mygenelog.com/variants/rs11919389