| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130057954, UNC45A (T2A) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130057954, UNC45A (R12P) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene