| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860734, POLE3 (R34W) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126860734, POLE3 (V27I) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126860734, POLE3 (P24L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene