| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Stickler Syndrome, Dominant +5 more | |
| | | Single nucleotide variant (missense variant) | Stickler Syndrome, Dominant +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Otospondylomegaepiphyseal dysplasia, autosomal recessive | |
| | | Duplication (frameshift variant) | See cases +1 more | |
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