RUNX1 and leukemia: Familial clusters of leukemia led to the identification of germline variants associated with lymphoid neoplasms (PAX5, IKZF1, SH2B3, and ARID2), myeloid neoplasms (RUNX1, GATA2, CEBPA, DDX41, ANKRD26, ETV6, and TP53), and inherited bone marrow syndromes (GATA2, TERC, TERT, FANCA, and FANCB) (31).