| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126806104, TPO (W829C +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806104, TPO (R702H +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806104, TPO (P892H +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene