Clinically relevant germline variants in allogeneic hematopoietic stem cell transplant recipients.
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ABSTRACT: Allogeneic hematopoietic stem cell transplantation (HSCT) provides patients with severe hematologic disease a well-established potential for curation. Incorporation of germline analyses in the workup of HSCT patients is not a common practice. Recognizing rare harmful germline variants may however affect patients' pre-transplantation care, choice of the stem cell donor, and complication risks. We analyzed a population-based series of germline exome data of 432 patients who had undergone HSCT. Our aim was to identify clinically relevant variants that may challenge the outcome of the HSCT. We focused on genes predisposing to hematological diseases, or solid tumors, and genes included in the American College of Medical Genetics secondary findings list v3.0. As population-specific controls, we
SUBMITTER: Lahtinen AK
PROVIDER: S-EPMC9812774 | biostudies-literature | 2023 Jan
REPOSITORIES: biostudies-literature
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