When the groups were evaluated in terms of pathological somatic gene variants, the most common pathogenic gene variants in AML patients in the young group were NF1 (6.3%), BLM (5%), KMT2C (Exon18 c.2961C>G (3.6%), and Exon8 c.1042G>A (3.8%)) variants. Here, BLM is linked to acute myeloid leukemia.