| | | Duplication (nonsense) | not provided +2 more | |
| | | Deletion (frameshift variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Duplication (frameshift variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (nonsense) | Fraser syndrome 2 | |
| | | Duplication (frameshift variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | Isolated cryptophthalmia +2 more | |
| | | Single nucleotide variant (synonymous variant) | Fraser syndrome 2 +3 more | |
| | | Insertion (intron variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Isolated cryptophthalmia +2 more | |
| | | Single nucleotide variant (missense variant) | Isolated cryptophthalmia +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Isolated cryptophthalmia +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +4 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Isolated cryptophthalmia +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Isolated cryptophthalmia +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (intron variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (nonsense) | Fraser syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | Fraser syndrome 2 +3 more | |
| | | Duplication (splice donor variant) | Fraser syndrome 1 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Microsatellite (frameshift variant) | Fraser syndrome 2 | |
| | | Duplication (frameshift variant) | Fraser syndrome 2 +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (nonsense) | Fraser syndrome 2 | |
| | | Indel (frameshift variant) | Fraser syndrome 2 | |
| | | Deletion (frameshift variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | Fraser syndrome 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Isolated cryptophthalmia +3 more | |
| | | Single nucleotide variant (intron variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | Fraser syndrome 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | FREM2-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | FREM2-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fraser syndrome 2 | |