RSF1 · rs146072725
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 26 Vis (founder/genetic isolate) cases, 36 Korculan (founder/genetic isolate) cases, 25 Split cases, 934 Vis (founder/genetic isolate) controls, 2,662 Korculan (founder/genetic isolate) controls, 941 Split controls.
The effect Each copy of the T allele carried 1.13 times the odds of Systemic infections (95% confidence interval 1.09-1.16); p = 8 × 10−13.
How common The T allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 11, band 11q14.1 — in an intron of RSF1.
rs146072725 is a single position in the genome, in or near the RSF1 gene. Published research associates it with systemic infections. 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, International journal of molecular sciences 2023, PMID:37108169. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Systemic infections (rs146072725). MyGeneLog™. https://www.mygenelog.com/variants/rs146072725