Genes closest to the association peaks were enriched for genes regulating haematological functions 14, 15, and for genes causative for Mendelian blood disorders (Tables S1–S2) such as haemolytic anaemia (HK1, G6PD), sickle cell disease (BCL11A, HBB, HBSx1L‐MYB), thrombocytopenia (MPL), leukaemia (PTPN11) and bone marrow failure (TERT). This evidence concerns the gene PTPN11 and non-autoimmune hemolytic anemia.