| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC112840921, OTOF (R1680C +2 more) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | LOC112840921, OTOF (R1676C +2 more) | Single nucleotide variant (missense variant) | not specified +2 more | |
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