| | | Single nucleotide variant (missense variant) | Bronchopulmonary dysplasia of newborn +9 more | |
| | | Single nucleotide variant (missense variant) | Anemia +9 more | |
| | | | Amyloidosis, hereditary systemic 1 | |
| | | Single nucleotide variant (missense variant) | Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 +7 more | |
| | | Single nucleotide variant (missense variant) | Anemia +1 more | |
| | APLP2, LINC02873 +169 more | Deletion | Anemia +7 more | |
| | | Single nucleotide variant (splice donor variant) | Pure red-cell aplasia +1 more | |
| | | Single nucleotide variant (splice donor variant) | SPTA1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome +1 more | |
| | | Duplication (frameshift variant) | Anemia +1 more | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental delay +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Anemia +4 more | |
| | HBB, LOC106099062 +1 more (E7V +1 more) | Single nucleotide variant (missense variant) | HEMOGLOBIN JAMAICA PLAIN | |
| | LOC106099062, LOC107133510 +1 more (E91K +1 more) | Single nucleotide variant (missense variant) | HEMOGLOBIN S (CAMEROON) | |
| | HBB, LOC107133510 +2 more (E122Q +1 more) | Single nucleotide variant (missense variant) | HEMOGLOBIN T (CAMBODIA) | |
| | HBB, LOC106099062 +2 more (E7V +1 more) | Single nucleotide variant (missense variant) | HEMOGLOBIN S (TRAVIS) | |
| | HBB, LOC106099062 +1 more (K83N +1 more) | Single nucleotide variant (missense variant) | HEMOGLOBIN S (PROVIDENCE) | |
| | HBB, LOC107133510 +2 more (E122K +1 more) | Single nucleotide variant (missense variant) | Sickle cell-Hemoglobin O Arab disease | |
| | HBB, LOC106099062 +1 more (E7V +1 more) | Single nucleotide variant (missense variant) | HEMOGLOBIN S (ANTILLES) | |
| | HBB, LOC106099062 +1 more (E7V +1 more) | Single nucleotide variant (missense variant) | HEMOGLOBIN ZIGUINCHOR | |
| | HBB, LOC106099062 +1 more (D74N +1 more) | Single nucleotide variant (missense variant) | HEMOGLOBIN ZIGUINCHOR | |
| | | Single nucleotide variant (missense variant) | Bone marrow hypocellularity +6 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spherocytosis type 1 | |
| | | Translocation | Clinodactyly of the 5th finger +14 more | |
| | | Single nucleotide variant (missense variant) | Splenomegaly +1 more | |
| | HBB, LOC106099062 +1 more (E7V) | Single nucleotide variant (missense variant) | beta Thalassemia +15 more | |
| | HBB, LOC106099062 +1 more (E27K) | Single nucleotide variant (missense variant) | Inborn genetic diseases +15 more | |
| | | Deletion | Anemia +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +12 more | |