| | | Single nucleotide variant (intron variant) | PITX2-Related Eye Abnormalities +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Irido-corneo-trabecular dysgenesis +6 more | |
| | | Single nucleotide variant (intron variant) | PITX2-Related Eye Abnormalities +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +7 more | |
| | | Single nucleotide variant (intron variant) | PITX2-Related Eye Abnormalities +7 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | PITX2-Related Eye Abnormalities +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Hypoplasia of the iris +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | PITX2-Related Eye Abnormalities +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Irido-corneo-trabecular dysgenesis +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Irido-corneo-trabecular dysgenesis +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Irido-corneo-trabecular dysgenesis +6 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hypoplasia of the iris +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | PITX2-Related Eye Abnormalities +6 more | |
| | | Single nucleotide variant (missense variant) | PITX2-Related Eye Abnormalities +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | PITX2-Related Eye Abnormalities +6 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Hypoplasia of the iris +6 more | |
| | | Single nucleotide variant (intron variant) | Ring dermoid of cornea +7 more | |
| | | Single nucleotide variant (intron variant) | Ring dermoid of cornea +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Ring dermoid of cornea +6 more | |
| | | Single nucleotide variant (intron variant) | Ring dermoid of cornea +6 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Ring dermoid of cornea +6 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Ring dermoid of cornea +6 more | |
| | | Single nucleotide variant (intron variant) | PITX2-Related Eye Abnormalities +6 more | |
| | | Single nucleotide variant (missense variant) | Anterior segment dysgenesis 4 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Anterior segment dysgenesis 1 +7 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Cataract +6 more | |
| | | Single nucleotide variant (synonymous variant) | Hypoplasia of the iris +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +6 more | |
| | | Microsatellite (3 prime UTR variant) | Cataract +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract +6 more | |
| | | Single nucleotide variant (synonymous variant) | Anterior segment dysgenesis 4 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +9 more | |
| | | Single nucleotide variant (missense variant) | Cataract +8 more | |
| | | Single nucleotide variant (intron variant) | Cataract +8 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Anterior segment dysgenesis 1 +7 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +9 more | |
| | | Single nucleotide variant (missense variant) | Axenfeld-Rieger syndrome type 1 +1 more | GPathogenic/Likely pathogenic |