| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CDH23, LOC111982869 (Y396N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CDH23, LOC111982869 (N2658H +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | CDH23, LOC111982869 (V2686A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
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