| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (inframe_deletion +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Usher syndrome | |
| | | Single nucleotide variant (missense variant) | X-linked dominant chondrodysplasia, Chassaing-Lacombe type | |
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