Sensitive

Peptic ulcer disease

TTC33 · rs6860328

Where this position leads

Condition: Peptic Ulcer Disease

rs6860328 Condition: Peptic Ulcer Disease Peptic Ulcer Disease Condition rs6860328 rs6860328 TTC33

What the study found

Who was studied 29,739 Japanese ancestry cases, 240,675 Japanese ancestry controls.

The effect Each copy of the C allele shifted the measure 0.0833 higher (95% confidence interval 0.065-0.101); p = 4 × 10−20.

How common The C allele had a frequency of about 58% in the people studied.

Where it sits Chromosome 5, band 5p13.1 — in an intron of TTC33.

What each result means

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

Questions about rs6860328

What is rs6860328?

rs6860328 is a single position in the genome, in or near the TTC33 gene. Published research associates it with peptic ulcer 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 rs6860328 linked to?

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

Does having rs6860328 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 rs6860328 come from?

GWAS Catalog, Nature genetics 2023, PMID:38036781. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Peptic ulcer disease (rs6860328). MyGeneLog™. https://www.mygenelog.com/variants/rs6860328

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