| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Denticles +4 more | |
| | | Deletion (frameshift variant) | Dentinogenesis imperfecta type 2 +4 more | GPathogenic/Likely pathogenic |
| | | Indel (missense variant) | Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 +3 more | |
Click to view in NCBI Gene