Particularly interesting for us were genes associated with clinical phenotypes of known inherited hemolytic anemia [6], including erythrocyte membranopathies (ANK1, SPTB, SPTA1, SLC4A1, EPB42, EPB41, PIEZO1, KCNN4, RHAG), erythrocyte enzymopathies (G6PD, PKLR, ENO1, AK1, GPI, NT5C3A, GCLC, GPX1, GSR, GSS, HK1, BPGM, PGK1, TPI1), and erythrocyte hemoglobinopathies (HBB, HBA1, HBA2). Here, G6PD is linked to hemoglobinopathy.