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Results of whole exome sequencing analysis of 55 patients with inherited thrombocytopenia showing variants in known thrombocytopenia-causing genes. 68% of individuals have a predicted genetic etiology in a previously IT-associated gene. When a variant has been previously observed it is annotated in the prevalence column with the database in which it is included. The ACMG consensus guideline results are also displayed in the final classification column.17
