| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Deletion (frameshift variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome +1 more | |
| | | Single nucleotide variant (nonsense) | Matthew-Wood syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (nonsense) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Duplication (frameshift variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Deletion (frameshift variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Matthew-Wood syndrome | |
| | | Microsatellite (splice donor variant) | Matthew-Wood syndrome | |
| | | Deletion (frameshift variant +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | STRA6-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | STRA6-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | STRA6-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | STRA6-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Matthew-Wood syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Indel (missense variant) | Matthew-Wood syndrome | |
| | | Duplication (frameshift variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | STRA6-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Deletion (intron variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (nonsense) | Matthew-Wood syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | STRA6-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Matthew-Wood syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | |
| | | Single nucleotide variant (missense variant) | Matthew-Wood syndrome | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | STRA6-related disorder +2 more | |
| | | Single nucleotide variant (intron variant +1 more) | Matthew-Wood syndrome | |