| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HBB, LOC106099062
+1 more (Q40*) | Single nucleotide variant (nonsense) | Inborn genetic diseases +11 more | |
| | HBB, LOC106099062
+1 more (E27K) | Single nucleotide variant (missense variant) | not provided +17 more | |
| | HBB, LOC106099062
+1 more (E7V) | Single nucleotide variant (missense variant) | See cases +16 more | |
| | HBB, LOC106099062
+1 more (E7K) | Single nucleotide variant (missense variant) | Inherited hemoglobinopathy +15 more | GPathogenic/Likely pathogenic |
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