| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129998914, STAG3 (S563Y +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998914, STAG3 (D571N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998914, STAG3 (P582R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene