| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC112840921, OTOF (L1032R +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC112840921, OTOF (T1720M +2 more) | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | LOC112840921, OTOF (M943L +2 more) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | LOC112840921, OTOF (R913S +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC112840921, OTOF (A987T +2 more) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | LOC112840921, OTOF (D906N +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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