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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 33,598 Korean ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.053 higher (95% confidence interval 0.045-0.061); p = 5 × 10−37.
Where it sits Chromosome 2, band 2q37.1 — in an intron of ATG16L1.
What each result means
A/ATwo copies of the version the research linked to Bilirubin levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Bilirubin levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Bilirubin levels. This is the starting point the study compared everyone against.
Epidemiology and health · 2019 · PMID 31319653 · open access
Questions about rs2119503
What is rs2119503?
rs2119503 is a single position in the genome, in or near the ATG16L1 gene. Published research associates it with bilirubin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2119503 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 rs2119503 come from?
GWAS Catalog, Epidemiology and health 2019, PMID:31319653. 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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