| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Osteogenesis imperfecta type 8 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Osteogenesis imperfecta +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | P3H1-related condition +3 more | |
| | | Single nucleotide variant (synonymous variant) | Osteogenesis imperfecta type 8 +1 more | |
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