| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR3-related disoder +14 more | |
| | | Single nucleotide variant (intron variant) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +15 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +14 more | |
| | HRAS, LRRC56 (R164P +1 more) | Single nucleotide variant (missense variant +1 more) | Large congenital melanocytic nevus +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Megalencephaly-capillary malformation-polymicrogyria syndrome +2 more | |
| | HRAS, LRRC56 (T31P +1 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | HRAS, LRRC56 (R161C +1 more) | Single nucleotide variant (missense variant +1 more) | Linear nevus sebaceous syndrome +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cowden syndrome +14 more | |
| | | Single nucleotide variant (missense variant) | not provided +16 more | |
| | | Single nucleotide variant (missense variant +2 more) | Crouzon syndrome-acanthosis nigricans syndrome +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome +6 more | |
| | | Single nucleotide variant (missense variant) | RASopathy +8 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +14 more | |
| | | Single nucleotide variant (intron variant) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome +14 more | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (missense variant +2 more) | Achondroplasia | |
| | | Single nucleotide variant (missense variant) | Seborrheic keratosis +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Large congenital melanocytic nevus +6 more | |
| | | Single nucleotide variant (missense variant) | Congenital macrodactylia +14 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Crouzon syndrome-acanthosis nigricans syndrome +16 more | |
| | HRAS, LRRC56 (R169Q +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | LRRC56, HRAS (R169W +1 more) | Single nucleotide variant (missense variant +1 more) | Linear nevus sebaceous syndrome +7 more | |
| | | Single nucleotide variant (missense variant +2 more) | Connective tissue disorder +16 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Crouzon syndrome-acanthosis nigricans syndrome +16 more | |
| | | Single nucleotide variant (stop lost +2 more) | Crouzon syndrome-acanthosis nigricans syndrome +14 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Noonan syndrome and Noonan-related syndrome +8 more | |
| | HRAS, LRRC56 (P174S +1 more) | Single nucleotide variant (missense variant +1 more) | RASopathy | |
| | HRAS, LRRC56 (K170* +1 more) | Single nucleotide variant (nonsense +1 more) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cowden syndrome +17 more | |
| | | Single nucleotide variant (missense variant) | NRAS-related condition +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Epidermal nevus | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome and Noonan-related syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +14 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +25 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Connective tissue disorder +17 more | |
| | | Single nucleotide variant (missense variant +1 more) | Connective tissue disorder +18 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (stop lost +2 more) | Achondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR3-related chondrodysplasia +32 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR3-Related Disorders +18 more | |
| | | Single nucleotide variant (missense variant) | Large congenital melanocytic nevus +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Melanoma +26 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Epidermal nevus +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | HRAS-related condition +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | HRAS-related condition +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |