| | | Single nucleotide variant (missense variant +1 more) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome | |
| | | 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 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +15 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice donor variant) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Crouzon syndrome-acanthosis nigricans syndrome +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Achondroplasia +14 more | |
| | | Single nucleotide variant (intron variant) | Achondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +2 more) | Achondroplasia | |
| | | Single nucleotide variant (synonymous variant +1 more) | Achondroplasia +16 more | |
| | | Single nucleotide variant (missense variant +1 more) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Achondroplasia +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) | Achondroplasia +16 more | |
| | | Single nucleotide variant (stop lost +2 more) | Achondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR3-related chondrodysplasia +25 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | FGFR3-related condition +17 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +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 | |