| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130060427, TOP3A (A50V) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC130060427, TOP3A (V36L) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene