The aim of the study is to investigate the existence of clonal hematopoiesis of indeterminate potential (CHIP) in patients with a history of venous thromboembolism. The study investigators make the assumption that these patients present mutations involved in CHIP occurrence.
Study Type
OBSERVATIONAL
Enrollment
150
CHU de Nimes
Nîmes, France
DNMT3A mutations screening
Next generation sequencing
Time frame: For sequencing analysis: 2 months
TET2, ASXL1, TP53, JAK2, SF3B1, SRSF2, GNB1, CBL, BCOR, SH2B3, PPM1D mutations screening
Next generation sequencing
Time frame: For sequencing analysis: 2 months
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