| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | HBA2, LOC106804612 (C105Y) | Single nucleotide variant (missense variant) | Hemoglobin H disease +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (stop lost) | not provided +2 more | |
Click to view in NCBI Gene