| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Duplication (intron variant) | UGP2-related disorder | |
| | | Single nucleotide variant (missense variant) | UGP2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | UGP2-related disorder | |
Click to view in NCBI Gene