| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 | |
| | | Duplication (inframe insertion +1 more) | Noonan syndrome 5 | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 | |
| | | Indel (missense variant +1 more) | Noonan syndrome 5 | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Noonan syndrome 5 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant +3 more) | RASopathy +2 more | |
| | LOC129936178, LOC129936179 +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 (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 | Noonan syndrome 5 +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) | RASopathy +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) | RASopathy +3 more | |
| | | Deletion (frameshift variant +2 more) | Noonan syndrome 5 | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Noonan syndrome +5 more | |
| | | Deletion (inframe_deletion +1 more) | not specified +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +4 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | LEOPARD syndrome 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Noonan syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (missense variant +2 more) | RASopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 2 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +2 more | GConflicting classifications of pathogenicity |
| | | 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) | not provided +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) | not provided +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) | not provided +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) | RASopathy +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | Noonan syndrome 5 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +7 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) | Noonan syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 5 +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) | not specified +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 5 | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1NN +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |