| | | Single nucleotide variant | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Duplication (5 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Deletion (5 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Duplication (5 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Duplication (5 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Insertion (5 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Duplication (5 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Duplication (5 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Single nucleotide variant (missense variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion (inframe_deletion) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Multiple synostoses syndrome 3 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Inversion (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Multiple synostoses syndrome 3 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | FGF9-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Microsatellite (3 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Deletion (3 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Deletion (3 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Deletion (3 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Microsatellite (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (3 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Microsatellite (3 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Microsatellite (3 prime UTR variant) | Symphalangism-brachydactyly syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple synostoses syndrome 3 | |