Fig. 4From: Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in TanzaniaBiological sub-network of the candidate mutant gene and identified modifier genes in 14 SCD patients from Tanzania. a sub-networks of our target sequencing variants include ZBTB7A, BCL11A, MYB, HBB, HOXA9, HBG2, CHD4, KLF1, MBD3.b description of the top most significant pathways, GO biological process, and Human Phenotypes associated with the identified variantsBack to article page