| | | Single nucleotide variant (missense variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +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) | Achondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Muenke syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not specified +15 more | |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases +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 +2 more) | not specified +16 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +15 more | |
| | | Single nucleotide variant (stop lost +2 more) | Achondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +14 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Hypochondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Craniosynostosis syndrome +26 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | FGFR3-related disorder +17 more | |
| | | Single nucleotide variant (missense variant +1 more) | Achondroplasia +18 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (stop lost +2 more) | Achondroplasia +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Lower limb undergrowth +31 more | |
| | | Single nucleotide variant (missense variant +2 more) | Achondroplasia +18 more | |