Investigating genetic factors that increase the risk of blood clots.

Structural and Nucleotide Variation as Genomic Risks for Venous Thrombosis: TOPMED and INVENT Collaboration

NIH-funded research University of Washington · NIH-10652342

This study is looking at how certain genetic differences might increase the risk of blood clots, like deep vein thrombosis and pulmonary embolism, and if you join, you can help researchers find out more about these genetic factors by providing a sample.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Washington NIH-funded
Lab location1 site (Seattle, United States)
Project IDNIH-10652342 on NIH RePORTER

What this research studies

This research focuses on understanding how genetic variations contribute to venous thromboembolism (VTE), a condition that can lead to serious complications like deep vein thrombosis and pulmonary embolism. By utilizing advanced whole-genome sequencing techniques, the study aims to identify rare genetic mutations and structural variations that may elevate the risk of developing VTE. Patients may be involved in providing genetic samples, which will help researchers uncover new insights into the genetic basis of this condition. The collaboration between multiple research groups enhances the potential for significant findings that could improve patient outcomes.

Who could benefit from this research

Good fit: Ideal candidates for participation include individuals with a family history of venous thromboembolism or those who have experienced blood clotting issues themselves.

Not a fit: Patients without a genetic predisposition to venous thromboembolism or those who have not experienced any related health issues may not benefit from this research.

Why it matters

Potential benefit: If successful, this research could lead to better risk assessment and personalized treatment strategies for patients at risk of blood clots.

How similar studies have performed: Previous research has shown promising results in identifying genetic factors associated with venous thromboembolism, indicating that this approach has potential for success.

Where this research is happening

Seattle, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.