| | CCDC146, CCDC201 +4735 more | Copy number loss | See cases | |
| | LOC129998995, LOC129998996 +2212 more | Copy number gain | See cases | |
| | LOC129999548, LOC129999549 +1547 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | TMEM139-AS1, TMEM140 +1052 more | Copy number gain | See cases | |
| | MIR5707, MIR595 +1046 more | Copy number gain | See cases | |
| | LOC123956245, LOC123956246 +1025 more | Copy number gain | See cases | |
| | LOC285889, LOC349160 +1025 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129999467, LOC129999468 +944 more | Copy number loss | See cases | |
| | LOC123956263, LOC126860190 +455 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129999526, LOC129999527 +908 more | Copy number gain | See cases | |
| | | Copy number gain | Neurodevelopmental disorder | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Neurodevelopmental disorder | |
| | | Copy number gain | See cases | |
| | BRAF, LOC126860202 +4 more | Copy number gain | See cases | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 7 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 7 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 7 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome 7 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 3 +1 more | |
| | BRAF, LOC126860202 +3 more | Duplication | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | LEOPARD syndrome 3 +1 more | |
| | | Deletion (inframe_deletion +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 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Deletion (frameshift variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Indel (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | 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 (synonymous variant +1 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 7 +7 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 3 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Deletion (intron variant +1 more) | Hypertrophic cardiomyopathy 4 | |
| | | Deletion (intron variant +1 more) | not provided | |
| | | Duplication (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Deletion (intron variant) | Cardio-facio-cutaneous syndrome +2 more | |
| | | Duplication (intron variant) | Cardio-facio-cutaneous syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | BRAF-related condition | |
| | | Microsatellite (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy +1 more | |
| | | Deletion (intron variant) | Cardio-facio-cutaneous syndrome +5 more | |
| | | Microsatellite (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Deletion (intron variant) | Noonan syndrome and Noonan-related syndrome +3 more | |
| | | Deletion (intron variant) | RASopathy | |
| | | Deletion (intron variant) | RASopathy | |
| | | Insertion (intron variant) | Cardiofaciocutaneous syndrome 1 +8 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Deletion (intron variant) | BRAF-related condition +1 more | |
| | | Indel (intron variant) | RASopathy +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Deletion (intron variant) | Cardio-facio-cutaneous syndrome +2 more | |
| | | Indel (intron variant) | not specified | |
| | | Deletion (intron variant) | not specified | |
| | | Duplication (intron variant) | RASopathy +2 more | |
| | | Indel (intron variant) | Cardio-facio-cutaneous syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Deletion (intron variant) | RASopathy | |
| | | Single nucleotide variant (intron variant) | RASopathy | |