| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | EXOSC3, LOC130001814 (P91T) | Single nucleotide variant (missense variant) | not provided | |
| | EXOSC3, LOC130001814 (C83G) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
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