| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Noonan syndrome 12 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | RRAS2-related condition +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (intron variant +1 more) | Noonan syndrome 12 +3 more | |
Click to view in NCBI Gene