| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Duplication (inframe_insertion) | Brachydactyly type D +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Brachydactyly type D +5 more | |
| | | Single nucleotide variant (missense variant) | HOXD13-related disorder +6 more | |
| | | Single nucleotide variant (nonsense) | Synpolydactyly +13 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene