| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 2 +2 more | |
| | LOC129936179, LOC129936180 +10 more | Duplication | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (intron variant +1 more) | Noonan syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | RASopathy +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 2 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | LEOPARD syndrome 2 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Dilated cardiomyopathy 1NN +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Noonan syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Dilated cardiomyopathy 1NN +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | Noonan syndrome 5 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Dilated cardiomyopathy 1NN +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | RAF1-related condition +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | LEOPARD syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RAF1-related condition +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RAF1-related condition +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | RASopathy +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | RASopathy | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | RASopathy | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified +3 more | |
| | | Microsatellite | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome | |