Sensitive

Crohn's disease

near NKX2-3 · rs10786560

Where this position leads

Condition: Crohn's Disease

rs10786560 Condition: Crohn's Disease Crohn's Disease Condition rs10786560 rs10786560 near NKX2-3

What the study found

Who was studied 2,523 Korean ancestry cases, 76,598 Korean ancestry controls.

The effect Each copy of the A allele carried 1.33 times the odds of Crohn's disease (95% confidence interval 1.23-1.44); p = 1 × 10−12.

How common The A allele had a frequency of about 30% in the people studied.

Where it sits Chromosome 10, band 10q24.2 — between genes, 18.9 kb from NKX2-3.

What each result means

A/A Two 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/G One copy of the version the research linked to Crohn's disease. That is a smaller link than two copies.
G/G No copy of the version the research linked to Crohn's disease. This is the starting point the study compared everyone against.
Source

Questions about rs10786560

What is rs10786560?

rs10786560 is a single position in the genome, in or near the near NKX2-3 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 rs10786560 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 rs10786560 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 rs10786560 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.

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.

Crohn's disease (rs10786560). MyGeneLog™. https://www.mygenelog.com/variants/rs10786560

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