near LINC01020 · rs570260
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 62,637 European ancestry cases, 313,185 European ancestry controls.
The effect Each copy of the G allele carried 1.03 times the odds of Hernia (any subtypes) (95% confidence interval 1.02-1.05); p = 6 × 10−10.
How common The G allele had a frequency of about 34% in the people studied.
Where it sits Chromosome 5, band 5p15.32 — between genes, 106 kb from LINC01020.
rs570260 is a single position in the genome, in or near the near LINC01020 gene. Published research associates it with hernia (any subtypes). 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, PloS one 2022, PMID:36584111. 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.
Hernia (any subtypes) (rs570260). MyGeneLog™. https://www.mygenelog.com/variants/rs570260