| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Indel | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | HBB, LOC107133510 +1 more (G137D) | Single nucleotide variant (missense variant) | beta Thalassemia +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +10 more | |
| | | Single nucleotide variant (synonymous variant) | Hemoglobin E +6 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene