SLC26A9 · rs4077468
Where this position leads
Condition: Cystic Fibrosis
What the study found
Who was studied 644 cystic fibrosis-related diabetes cases, 2,415 cystic fibrosis controls; replicated in 124 cystic fibrosis-related diabetes cases, 570 cystic fibrosis controls.
The effect Each copy of the A allele carried 1.39 times the odds of Cystic fibrosis-related diabetes (95% confidence interval 1.25-1.54); p = 1 × 10−9.
How common The A allele had a frequency of about 58% in the people studied.
Where it sits Chromosome 1, band 1q32.1 — inside SLC26A9-AS1.
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.
rs4077468 is a single position in the genome, in or near the SLC26A9 gene. Published research associates it with cystic fibrosis-related diabetes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Cystic Fibrosis. The research behind each link, and its sources, are set out on that condition page.
Subjects that appear in the title or abstract of the same papers as this rsID include gut and food intolerance (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, Diabetes 2013, PMID:23670970. 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.
Cystic fibrosis-related diabetes (rs4077468). MyGeneLog™. https://www.mygenelog.com/variants/rs4077468