Associated Genetic Biomarkers
JAK2 R683G is present in 0.00% of AACR GENIE cases, with leukemia having the greatest prevalence .
JAK2 R683G serves as an inclusion eligibility criterion in 1 clinical trial, of which 0 are open and 1 is closed. Of the trial that contains JAK2 R683G as an inclusion criterion, 1 is phase 1 (0 open).
Trials with JAK2 R683G in the inclusion eligibility criteria most commonly target myelodysplastic syndromes .
Significance of JAK2 R683G in Diseases
Myelodysplastic Syndromes +
JAK2 is mutated in 4.82% of myelodysplastic syndromes patients .
JAK2 R683G is an inclusion criterion in 1 clinical trial for myelodysplastic syndromes, of which 0 are open and 1 is closed. Of the trial that contains JAK2 R683G and myelodysplastic syndromes as inclusion criteria, 1 is phase 1 (0 open) .
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4. The AACR Project GENIE Consortium. AACR Project GENIE: powering precision medicine through an international consortium. Cancer Discovery. 2017;7(8):818-831. Dataset Version 4. This dataset does not represent the totality of the genetic landscape; see paper for more information.