Sensitive

Inflammatory bowel disease

LINC00598 · rs17061048

Where this position leads

Condition: Inflammatory Bowel Disease

rs17061048 Condition: Inflammatory Bowel Disease Inflammatory Bowel Disease Condition rs17061048 rs17061048 LINC00598

What the study found

Who was studied 12,882 European ancestry cases, 21,770 European ancestry controls; replicated in 25,273 European ancestry cases, 26,715 European ancestry controls, 548 Iranian ancestry cases, 342 Iranian ancestry control, 1,423 Indian ancestry cases, 990 Indian ancestry controls, 2,824 East Asian ancestry cases, 3,719 East Asian ancestry controls.

The effect The reported allele is A; the catalogue records no effect size ; p = 5 × 10−9.

How common The A allele had a frequency of about 95% in the people studied.

Where it sits Chromosome 13, band 13q14.11 — in an intron of LINC00598.

What each result means

A/A Two copies of the version the research linked to Inflammatory bowel disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/T One copy of the version the research linked to Inflammatory bowel disease. That is a smaller link than two copies.
T/T No copy of the version the research linked to Inflammatory bowel disease. This is the starting point the study compared everyone against.
Source

Questions about rs17061048

What is rs17061048?

rs17061048 is a single position in the genome, in or near the LINC00598 gene. Published research associates it with inflammatory bowel 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 rs17061048 linked to?

On MyGeneLog this position is linked to Inflammatory Bowel Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs17061048 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 rs17061048 come from?

GWAS Catalog, Nature genetics 2015, PMID:26192919. 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.

Inflammatory bowel disease (rs17061048). MyGeneLog™. https://www.mygenelog.com/variants/rs17061048

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