| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC111721705, ZEB2 (N192S +1 more) | Single nucleotide variant (missense variant) | Mowat-Wilson syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Mowat-Wilson syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene