| | | Single nucleotide variant (missense variant) | Noonan syndrome 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Metachondromatosis +2 more | |
| | | Insertion (inframe_insertion) | Metachondromatosis | |
| | | Single nucleotide variant (missense variant) | Metachondromatosis | |
| | | Deletion (frameshift variant) | Metachondromatosis | |
| | | Single nucleotide variant (intron variant) | RASopathy +4 more | |
| | | Single nucleotide variant (synonymous variant) | RASopathy +4 more | |
| | | Single nucleotide variant (missense variant) | RASopathy +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | LEOPARD syndrome 1 +4 more | |
| | | Single nucleotide variant (missense variant) | LEOPARD syndrome 1 +4 more | |
| | | Single nucleotide variant (missense variant) | Juvenile myelomonocytic leukemia +4 more | |
| | | Single nucleotide variant (nonsense) | Noonan syndrome 1 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | LEOPARD syndrome 1 +4 more | |
| | | Single nucleotide variant (missense variant) | Juvenile myelomonocytic leukemia +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Metachondromatosis | |
| | | Single nucleotide variant (synonymous variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LEOPARD syndrome 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +7 more | |
| | | Deletion (frameshift variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant) | RASopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Noonan syndrome 1 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Noonan syndrome 1 +2 more | |
| | | Single nucleotide variant | LEOPARD syndrome 1 +2 more | |
| | | Deletion (frameshift variant) | Metachondromatosis | |
| | | Microsatellite (inframe_deletion) | PTPN11-related condition +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Metachondromatosis | |
| | | Single nucleotide variant (synonymous variant) | Juvenile myelomonocytic leukemia +7 more | |
| | | Single nucleotide variant (synonymous variant) | Noonan syndrome 1 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | Juvenile myelomonocytic leukemia +6 more | |
| | | Single nucleotide variant (synonymous variant) | RASopathy +5 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (synonymous variant) | RASopathy +6 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy +6 more | |
| | | Duplication (intron variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Microsatellite (3 prime UTR variant) | Noonan syndrome +2 more | |
| | | Microsatellite (3 prime UTR variant) | Noonan syndrome +2 more | |
| | | Microsatellite (3 prime UTR variant) | Metachondromatosis +2 more | |
| | | Microsatellite (3 prime UTR variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | LEOPARD syndrome 1 +2 more | |