| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Larsen-like syndrome, B3GAT3 type | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Larsen-like syndrome, B3GAT3 type +1 more | |
Click to view in NCBI Gene