| | | Single nucleotide variant (intron variant) | Achondroplasia +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hypochondroplasia | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +1 more | GConflicting classifications of pathogenicity |
| | | 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 +2 more) | not provided | |
| | | 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) | Hypochondroplasia | |
| | | Indel (missense variant +1 more) | Hypochondroplasia | |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +1 more | |
| | | 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 |
| | | 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) | not provided +14 more | |
| | | Single nucleotide variant (intron variant) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Thanatophoric dysplasia type 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Achondroplasia | |
| | | Single nucleotide variant (synonymous variant +1 more) | Crouzon syndrome-acanthosis nigricans syndrome +16 more | |
| | | Single nucleotide variant (missense variant +1 more) | Connective tissue disorder +3 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 (missense variant +2 more) | Hypochondroplasia | |
| | | Single nucleotide variant (stop lost +2 more) | Crouzon syndrome-acanthosis nigricans syndrome +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +14 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided | 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 (missense variant +1 more) | FGFR3-related condition +4 more | |
| | | 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 condition +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR3-Related Disorders +18 more | |