Standard

Hemorrhage from gastrointestinal ulcer (PheCode 531.1)

near YPEL5 · rs529776754

Where this position leads

Condition: Hemorrhage from Gastrointestinal Ulcer

rs529776754 Condition: Hemorrhage from Gastrointestinal Ulcer Hemorrhage from Gastrointestinal Ulcer Condition rs529776754 rs529776754 near YPEL5

What the study found

Who was studied 594 African American or Afro-Caribbean cases, 120,387 African American or Afro-Caribbean controls, 2,163 European ancestry cases, 446,114 European ancestry controls, 255 Hispanic or Latin American cases, 59,281 Hispanic or Latin American controls.

The effect Each copy of the C allele shifted the measure 1.77 lower (95% confidence interval 1.7-1.84); p = 3 × 10−11.

How common The C allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 2, band 2p23.1 — between genes, 31.1 kb from YPEL5.

What each result means

C/C Two copies of the version the research linked to Hemorrhage from gastrointestinal ulcer (PheCode 531.1). 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 Hemorrhage from gastrointestinal ulcer (PheCode 531.1). That is a smaller link than two copies.
T/T No copy of the version the research linked to Hemorrhage from gastrointestinal ulcer (PheCode 531.1). This is the starting point the study compared everyone against.
Source

Questions about rs529776754

What is rs529776754?

rs529776754 is a single position in the genome, in or near the near YPEL5 gene. Published research associates it with hemorrhage from gastrointestinal ulcer (phecode 531.1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs529776754 linked to?

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

Does having rs529776754 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 rs529776754 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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.

Hemorrhage from gastrointestinal ulcer (PheCode 531.1) (rs529776754). MyGeneLog™. https://www.mygenelog.com/variants/rs529776754

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