| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861959, PPM1A (G90E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861959, PPM1A (R23Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861959, PPM1A (Y97F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861959, PPM1A (S125L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861959, PPM1A (I79M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861959, PPM1A (R228S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861959, PPM1A (E229D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861959, PPM1A (D303N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene