| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant +2 more) | RASopathy +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | RASopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Indel (frameshift variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant) | RASopathy +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 +2 more | GConflicting classifications of pathogenicity |
| | | Indel (missense variant +2 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 +2 more | |
| | | Deletion (intron variant) | RASopathy +4 more | |
| | | Single nucleotide variant (intron variant +2 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (non-coding transcript variant +2 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (intron variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (intron variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Deletion (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Deletion (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Duplication (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Duplication (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Deletion (3 prime UTR variant +1 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +1 more | |
| | | Deletion (intron variant) | RASopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (synonymous variant +2 more) | RASopathy +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Noonan syndrome-like disorder with loose anagen hair 1 | |
| | | Single nucleotide variant (missense variant) | RASopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | SHOC2-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome and Noonan-related syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome and Noonan-related syndrome +2 more | |
| | | Deletion (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | Noonan syndrome-like disorder with loose anagen hair 1 +2 more | |
| | | Single nucleotide variant (intron variant) | Noonan syndrome-like disorder with loose anagen hair 1 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | Noonan syndrome-like disorder with loose anagen hair 1 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Noonan syndrome and Noonan-related syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Noonan syndrome-like disorder with loose anagen hair 1 | |