Fig. 3From: 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 the mutant gene and identified candidate genetic modifiers include CHD4 and MBD3. b description of the top most significant pathways, GO biological process, and Human Phenotypes associated with the identified variantsBack to article page