| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant +1 more) | PSTPIP1-related condition +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autoinflammatory syndrome +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene