| | | Single nucleotide variant (missense variant +1 more) | Bent bone dysplasia syndrome 1 +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (intron variant) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Familial scaphocephaly syndrome, McGillivray type +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Craniosynostosis syndrome +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Beare-Stevenson cutis gyrata syndrome +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I | |
| | | Single nucleotide variant (missense variant +2 more) | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Insertion | Acrocephalosyndactyly type I | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +11 more | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | FGFR2-related craniosynostosis +1 more | |
| | | Single nucleotide variant (intron variant) | Beare-Stevenson cutis gyrata syndrome +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis +11 more | |
| | | Single nucleotide variant (intron variant) | FGFR2-related craniosynostosis +11 more | |
| | | 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 +1 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) | Pfeiffer syndrome +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +13 more | |
| | | Single nucleotide variant (missense variant +1 more) | Jackson-Weiss syndrome +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pfeiffer syndrome +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Jackson-Weiss syndrome +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) | not provided +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) | Beare-Stevenson cutis gyrata syndrome +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) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Jackson-Weiss syndrome +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +1 more | |
| | | Deletion (frameshift variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +13 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 +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Beare-Stevenson cutis gyrata syndrome +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) | Acrocephalosyndactyly type I +12 more | |
| | | Single nucleotide variant (missense variant +2 more) | Saethre-Chotzen syndrome +12 more | GConflicting classifications of pathogenicity |
| | | 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) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FGFR2-related craniosynostosis +12 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Bent bone dysplasia syndrome 1 +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Bent bone dysplasia syndrome 1 +12 more | |
| | | Single nucleotide variant (missense variant +1 more) | Beare-Stevenson cutis gyrata syndrome +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Saethre-Chotzen syndrome +16 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FGFR2-related craniosynostosis +11 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Jackson-Weiss syndrome +12 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Jackson-Weiss syndrome +12 more | |