| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Noonan syndrome | |
| | | Single nucleotide variant (missense variant) | PTPN11-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Noonan syndrome with multiple lentigines | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome and Noonan-related syndrome +11 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome with multiple lentigines +8 more | |
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