| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126805805, PLPPR4 (A385V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805805, PLPPR4 (K501R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805805, PLPPR4 (A460S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene