| | | Single nucleotide variant (intron variant) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (intron variant) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Crouzon syndrome +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Beare-Stevenson cutis gyrata syndrome +12 more | |
| | | Indel (intron variant) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Jackson-Weiss syndrome +12 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Deletion (frameshift variant +2 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Beare-Stevenson cutis gyrata syndrome +13 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Craniosynostosis syndrome +12 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis +12 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FGFR2-related disorder +13 more | |
| | | Single nucleotide variant (missense variant +1 more) | Beare-Stevenson cutis gyrata syndrome +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | FGFR2-related craniosynostosis +13 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Bent bone dysplasia syndrome 1 +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not specified +13 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pfeiffer syndrome +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Crouzon syndrome +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Saethre-Chotzen syndrome +12 more | |
| | | Single nucleotide variant (intron variant) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Craniosynostosis syndrome +15 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pfeiffer syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +12 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | not provided +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | not provided +13 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | FGFR2-related craniosynostosis +15 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +13 more | GPathogenic/Likely pathogenic |