| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | WNT10A-related disorder +6 more | |
| | | Single nucleotide variant (missense variant) | SchC6pf-Schulz-Passarge syndrome +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene