Sensitive

Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment

near CA10 · rs967823

Where this position leads

Condition: Peptic Ulcer Disease

rs967823 Condition: Peptic Ulcer Disease Peptic Ulcer Disease Condition rs967823 rs967823 near CA10

What the study found

Who was studied 90,175 European ancestry cases, 366,152 European ancestry controls.

The effect The reported allele is A; the catalogue records no effect size ; p = 2 × 10−12.

How common The A allele had a frequency of about 61% in the people studied.

Where it sits Chromosome 17, band 17q22 — between genes, 79.9 kb from CA10.

What each result means

A/A Two copies of the version the research linked to Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment. 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 Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment. That is a smaller link than two copies.
G/G No copy of the version the research linked to Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment. This is the starting point the study compared everyone against.
Source

Questions about rs967823

What is rs967823?

rs967823 is a single position in the genome, in or near the near CA10 gene. Published research associates it with gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs967823 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 rs967823 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 rs967823 come from?

GWAS Catalog, Nature communications 2021, PMID:33608531. 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.

Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment (rs967823). MyGeneLog™. https://www.mygenelog.com/variants/rs967823

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