| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HBB, LOC106099062
+1 more (G70S) | Single nucleotide variant (missense variant) | beta Thalassemia +13 more | GConflicting classifications of pathogenicity |
| | HBB, LOC106099062
+1 more (E7V) | Single nucleotide variant (missense variant) | Inborn genetic diseases +16 more | |
| | | Copy number gain | not provided | |
Click to view in NCBI Gene