| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Deletion (nonsense) | Stickler syndrome type 1 | |
| | | Single nucleotide variant (splice acceptor variant) | Stickler syndrome type 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Spondyloperipheral dysplasia +14 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Stickler syndrome type 1 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Stickler syndrome type 1 +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice acceptor variant) | Otospondylomegaepiphyseal dysplasia, autosomal recessive | |
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