| | | Single nucleotide variant (missense variant +1 more) | FGFR3-related disoder +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Malignant tumor of urinary bladder +16 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +32 more | |
| | | Single nucleotide variant (missense variant +1 more) | Malignant tumor of urinary bladder +17 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +25 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases +18 more | |
| | | Single nucleotide variant (missense variant +2 more) | not specified +16 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +15 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +18 more | GPathogenic/Likely pathogenic |
| | | 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 (synonymous variant +1 more) | Camptodactyly-tall stature-scoliosis-hearing loss syndrome +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +16 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +14 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not provided +14 more | |
| | | Single nucleotide variant (intron variant) | Achondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +2 more) | Achondroplasia +14 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) | not provided +14 more | |
| | | Single nucleotide variant (stop lost +2 more) | Achondroplasia +14 more | |
| | | Single nucleotide variant (stop lost +2 more) | Epidermal nevus +14 more | |