| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | GAL3ST2, LOC110599582 (Q333L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GAL3ST2, LOC110599582 (M377L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GAL3ST2, LOC110599582 (P386R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene