| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Idiopathic hypereosinophilic syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | PDGFRA-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more | |
| | | Single nucleotide variant (missense variant) | Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more | |
| | LOC126807054, PDGFRA (L802P) | Single nucleotide variant (missense variant +1 more) | Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal | |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic hypereosinophilic syndrome +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene