Sensitive

Venous thromboembolism recurrence in unprovoked as first VTE

LINC01924 · rs148611543

Where this position leads

Condition: Venous Thromboembolism

rs148611543 Condition: Venous Thromboembolism Venous Thromboembolism Condition rs148611543 rs148611543 LINC01924

What the study found

Who was studied 969 European ancestry cases, 2,248 European ancestry controls.

The effect Each copy of the A allele carried 2.10 times the odds of Venous thromboembolism recurrence in unprovoked as first VTE (95% confidence interval 1.654209-2.656765); p = 9 × 10−10.

How common The A allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 18, band 18q22.1 — in an intron of LINC01924.

What each result means

A/A Two copies of the version the research linked to Venous thromboembolism recurrence in unprovoked as first VTE. 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 Venous thromboembolism recurrence in unprovoked as first VTE. That is a smaller link than two copies.
G/G No copy of the version the research linked to Venous thromboembolism recurrence in unprovoked as first VTE. This is the starting point the study compared everyone against.
Source

Questions about rs148611543

What is rs148611543?

rs148611543 is a single position in the genome, in or near the LINC01924 gene. Published research associates it with venous thromboembolism recurrence in unprovoked as first vte. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs148611543 linked to?

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

Does having rs148611543 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 rs148611543 come from?

GWAS Catalog, Blood 2025, PMID:40811855. 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.

Venous thromboembolism recurrence in unprovoked as first VTE (rs148611543). MyGeneLog™. https://www.mygenelog.com/variants/rs148611543

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