| | | Single nucleotide variant (missense variant) | Noonan-like syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome | |
| | | Duplication (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome 6 | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice donor variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant) | RASopathy +1 more | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | NRAS-related condition +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant) | RASopathy | |
| | | Microsatellite (inframe_insertion) | RASopathy | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (synonymous variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (nonsense) | RASopathy | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | RASopathy +1 more | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Duplication (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy +1 more | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Duplication (intron variant) | RASopathy | |
| | | Deletion (intron variant) | not specified +2 more | |