| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I | |
| | | Insertion | Acrocephalosyndactyly type I | |
| | | Single nucleotide variant (intron variant +1 more) | FGFR2-related craniosynostosis +1 more | |
| | | Single nucleotide variant (intron variant) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (intron variant) | FGFR2-related craniosynostosis +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) | Acrocephalosyndactyly type I +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) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +12 more | |
| | | Indel (intron variant) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | Acrocephalosyndactyly type I | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Beare-Stevenson cutis gyrata syndrome +12 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I +1 more | |
| | | Deletion (frameshift variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Acrocephalosyndactyly type I +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) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pfeiffer syndrome +13 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Pfeiffer syndrome +12 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +2 more | GConflicting classifications of pathogenicity |
| | | 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) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Jackson-Weiss syndrome +12 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Jackson-Weiss syndrome +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Beare-Stevenson cutis gyrata syndrome +13 more | |
| | | Single nucleotide variant (missense variant +1 more) | Crouzon syndrome +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Beare-Stevenson cutis gyrata syndrome +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +13 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-realated disorder +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) | not provided +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Saethre-Chotzen syndrome +13 more | |
| | | Single nucleotide variant (missense variant +1 more) | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis +12 more | GConflicting classifications of pathogenicity |
| | | Duplication (5 prime UTR variant +1 more) | Crouzon syndrome +8 more | |
| | | Microsatellite (intron variant) | Acrocephalosyndactyly type I +9 more | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant +2 more) | Crouzon syndrome +10 more | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant +1 more) | Crouzon syndrome +8 more | |
| | | Duplication (3 prime UTR variant +1 more) | Beare-Stevenson cutis gyrata syndrome +8 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Craniosynostosis syndrome +12 more | |
| | | Deletion (3 prime UTR variant +1 more) | Acrocephalosyndactyly type I +8 more | |
| | | Single nucleotide variant (intron variant) | Crouzon syndrome +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Craniosynostosis syndrome +15 more | |
| | | Indel (missense variant +2 more) | Acrocephalosyndactyly type I | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +12 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +12 more | |
| | | Insertion | Acrocephalosyndactyly type I | |
| | | Indel (missense variant +2 more) | Acrocephalosyndactyly type I | |
| | | Single nucleotide variant (missense variant +2 more) | Pfeiffer syndrome +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Pfeiffer syndrome +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | not provided +13 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pfeiffer syndrome +15 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pfeiffer syndrome +13 more | GPathogenic/Likely pathogenic |