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Who was studied 2,523 Korean ancestry cases, 76,598 Korean ancestry controls.
The effect
Each copy of the A allele carried 1.46 times the odds of Crohn's disease (95% confidence interval 1.34-1.59); p = 3 × 10−18.
How common The A allele had a frequency of about 20% in the people studied.
Where it sits Chromosome 4, band 4p14 — in an intron of LINC02513.
What each result means
A/ATwo copies of the version the research linked to Crohn's disease. 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 Crohn's disease. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Crohn's disease. This is the starting point the study compared everyone against.
Journal of Crohn's & colitis · 2024 · PMID 37523193
Questions about rs73243351
What is rs73243351?
rs73243351 is a single position in the genome, in or near the LINC02513 gene. Published research associates it with crohn's disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs73243351 linked to?
On MyGeneLog this position is linked to Crohn's Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs73243351 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 rs73243351 come from?
GWAS Catalog, Journal of Crohn's & colitis 2024, PMID:37523193. 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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