FAT3 · rs10765567
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 6,141 European ancestry cases, 59,475 European ancestry controls; replicated in 9,171 European ancestry cases, 406,168 European ancestry controls.
The effect Each copy of the A allele carried 1.14 times the odds of Retinal detachment or retinal break (95% confidence interval 1.11-1.18); p = 2 × 10−17.
How common The A allele had a frequency of about 63% in the people studied.
Where it sits Chromosome 11, band 11q14.3 — in an intron of FAT3.
rs10765567 is a single position in the genome, in or near the FAT3 gene. Published research associates it with retinal detachment or retinal break. 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, Human molecular genetics 2020, PMID:31816047. 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.
Retinal detachment or retinal break (rs10765567). MyGeneLog™. https://www.mygenelog.com/variants/rs10765567