| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130062155, PPP4R1 (Q12L) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC130062155, PPP4R1 (E9G) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene