NFIB · rs13286037
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 1,421 European ancestry cases, 154 Hispanic/Latino cases, 121 East Asian ancestry cases, 81,843 European ancestry controls, 8,406 Hispanic/Latino controls, 7,397 East Asian ancestry controls.
The effect Each copy of the A allele carried 1.63 times the odds of Ankle injury (95% confidence interval 1.46-1.8); p = 5 × 10−8.
How common The A allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 9, band 9p22.3 — in an intron of NFIB.
rs13286037 is a single position in the genome, in or near the NFIB gene. Published research associates it with ankle injury. 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 2017, PMID:28957384. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.