| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC124403906, TASOR2 (A1620P +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124403906, TASOR2 (E1706G +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124403906, TASOR2 (T1732M +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124403906, TASOR2 (V1655M +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene