| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130007649, LOC130007650 +1258 more | Copy number gain | See cases | |
| | LOC124625919, LOC124625920 +1009 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126861648, LOC126861649 +4836 more | Copy number gain | See cases | |
| | LOC130007425, LOC130007426 +1257 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129390413, LOC129390414 +133 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Duplication (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome and Noonan-related syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Deletion (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Deletion (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Duplication (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Duplication (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Deletion (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | RASopathy +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Duplication (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Insertion (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (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) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Deletion (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Duplication (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome and Noonan-related syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome and Noonan-related syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome and Noonan-related syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome | |
| | | Duplication | RASopathy | |
| | | Deletion | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided | |
| | | Deletion (3 prime UTR variant +1 more) | Cerebral arteriovenous malformation +13 more | |
| | | Deletion (3 prime UTR variant +1 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | RASopathy +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | RASopathy | |
| | | Microsatellite (3 prime UTR variant +1 more) | RASopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | RASopathy | |
| | | Deletion (3 prime UTR variant +1 more) | Toriello-Lacassie-Droste syndrome | |
| | | Microsatellite (3 prime UTR variant +1 more) | Primary familial hypertrophic cardiomyopathy | |