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Who was studied 1,115 European ancestry cases, 5,655 European ancestry controls.
The effect
The reported allele is T; the catalogue records no effect size
; p = 4 × 10−10.
How common The T allele had a frequency of about 11% in the people studied.
Where it sits Chromosome 13, band 13q12.12 — in an intron of ATP12A.
What each result means
C/CNo copy of the version the research linked to Meconium ileus in cystic fibrosis. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Meconium ileus in cystic fibrosis. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Meconium ileus in cystic fibrosis. That is the strongest link of the three results. A link in a study is not a diagnosis.
PLoS genetics · 2019 · PMID 30807572 · open access
Questions about rs61948108
What is rs61948108?
rs61948108 is a single position in the genome, in or near the ATP12A gene. Published research associates it with meconium ileus in cystic fibrosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs61948108 linked to?
On MyGeneLog this position is linked to Cystic Fibrosis. The research behind each link, and its sources, are set out on that condition page.
Does having rs61948108 mean I will get this?
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.
Where does the information about rs61948108 come from?
GWAS Catalog, PLoS genetics 2019, PMID:30807572. 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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Quoting this page
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.
Meconium ileus in cystic fibrosis (rs61948108). MyGeneLog™. https://www.mygenelog.com/variants/rs61948108