| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (stop lost) | Autosomal dominant Robinow syndrome 1 | |
| | | Duplication (frameshift variant) | Autosomal dominant Robinow syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
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