| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more | GConflicting classifications of pathogenicity |
| | LOC126807054, PDGFRA (T782M) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer +2 more | GConflicting classifications of pathogenicity |
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