| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126653386, PRDM15 (D205N +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126653386, PRDM15 (V104M +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126653386, PRDM15 (P103R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene