Gene Knowledge Graph
UTC
Standard

Hemorrhage from gastrointestinal ulcer (PheCode 531.1)

near LINC01951 · rs767453489

Where this position leads

Condition: Hemorrhage from Gastrointestinal Ulcer

rs767453489 Condition: Hemorrhage from Gastrointestinal Ulcer Hemorrhage from Gastrointestinal Ulcer Condition rs767453489 rs767453489 near LINC019…

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 G allele shifted the measure 2.38 lower (95% confidence interval 2.33-2.43); p = 3 × 10−11.

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

Where it sits Chromosome 5, band 5q35.2 — between genes, 12 kb from LINC01951.

What each result means

A/A 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.
A/G One copy of the version the research linked to Hemorrhage from gastrointestinal ulcer (PheCode 531.1). That is a smaller link than two copies.
G/G 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.
Source
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Verma A, Huffman JE, Rodriguez A, Conery M, Liu M, Ho YL, Kim Y, Heise DA, Guare L, Panickan VA, Garcon H, Linares F
and 59 more — show all
Costa L, Goethert I, Tipton R, Honerlaw J, Davies L, Whitbourne S, Cohen J, Posner DC, Sangar R, Murray M, Wang X, Dochtermann DR, Devineni P, Shi Y, Nandi TN, Assimes TL, Brunette CA, Carroll RJ, Clifford R, Duvall S, Gelernter J, Hung A, Iyengar SK, Joseph J, Kember R, Kranzler H, Kripke CM, Levey D, Luoh SW, Merritt VC, Overstreet C, Deak JD, Grant SFA, Polimanti R, Roussos P, Shakt G, Sun YV, Tsao N, Venkatesh S, Voloudakis G, Justice A, Begoli E, Ramoni R, Tourassi G, Pyarajan S, Tsao P, O'Donnell CJ, Muralidhar S, Moser J, Casas JP, Bick AG, Zhou W, Cai T, Voight BF, Cho K, Gaziano JM, Madduri RK, Damrauer S, Liao KP
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access

Questions about rs767453489

What is rs767453489?

rs767453489 is a single position in the genome, in or near the near LINC01951 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 rs767453489 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 rs767453489 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 rs767453489 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) (rs767453489). MyGeneLog™. https://www.mygenelog.com/variants/rs767453489

← See all variants