ABO · rs579459
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 685 European ancestry individuals with type 1 diabetes; replicated in 477 European ancestry individuals.
The effect The reported allele is C; the catalogue records no effect size ; p = 1 × 10−29.
How common The C allele had a frequency of about 20% in the people studied.
Where it sits Chromosome 9, band 9q34.2 — between genes, 2.7 kb from ABO.
What people read about alongside this
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
rs579459 is a single position in the genome, in or near the ABO gene. Published research associates it with soluble e-selectin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (10 papers), sleep and insomnia (3 papers), blood sugar and insulin (1 papers), cholesterol and blood fats (1 papers), liver (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
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, Arterioscler Thromb Vasc Biol 2009, PMID:19729612. 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.
Soluble E-selectin levels (rs579459). MyGeneLog™. https://www.mygenelog.com/variants/rs579459