| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130068266, OTUD5 (G112A) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130068266, OTUD5 (G110V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130068266, OTUD5 (G105A) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
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