Sensitive

Venous thromboembolism recurrence in pulmonary embolism as first VTE

SLC4A1 · rs45562031

Where this position leads

Condition: Venous Thromboembolism

rs45562031 Condition: Venous Thromboembolism Venous Thromboembolism Condition rs45562031 rs45562031 SLC4A1

What the study found

Who was studied 667 European ancestry cases, 2,065 European ancestry controls.

The effect Each copy of the T allele carried 3.13 times the odds of Venous thromboembolism recurrence in pulmonary embolism as first VTE (95% confidence interval 2.22701-4.411788); p = 6 × 10−11.

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

Where it sits Chromosome 17, band 17q21.31 — a missense change in SLC4A1.

What each result means

C/C No copy of the version the research linked to Venous thromboembolism recurrence in pulmonary embolism as first VTE. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Venous thromboembolism recurrence in pulmonary embolism as first VTE. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Venous thromboembolism recurrence in pulmonary embolism as first VTE. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs45562031

What is rs45562031?

rs45562031 is a single position in the genome, in or near the SLC4A1 gene. Published research associates it with venous thromboembolism recurrence in pulmonary embolism 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 rs45562031 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 rs45562031 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 rs45562031 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 pulmonary embolism as first VTE (rs45562031). MyGeneLog™. https://www.mygenelog.com/variants/rs45562031

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