| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant) | Axenfeld-Rieger syndrome type 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Axenfeld-Rieger syndrome type 3 +1 more | GConflicting classifications of pathogenicity |
| | FOXC1, LOC129995601 (T88I) | Single nucleotide variant (missense variant) | Axenfeld-Rieger syndrome type 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | FOXC1, LOC129995601 (K98fs) | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Axenfeld-Rieger syndrome type 3 +2 more | |
| | | Single nucleotide variant (missense variant) | Axenfeld-Rieger syndrome type 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Axenfeld-Rieger syndrome type 3 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Axenfeld-Rieger syndrome type 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion (inframe_deletion) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Axenfeld-Rieger syndrome type 3 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Axenfeld-Rieger syndrome type 3 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Microsatellite (inframe_insertion) | not specified +2 more | |
| | | Duplication (inframe_insertion) | not specified | |
| | | Microsatellite (inframe_insertion) | Anterior segment dysgenesis 3 +2 more | |
| | | Microsatellite (inframe_deletion) | Axenfeld-Rieger syndrome type 3 +2 more | |
| | | Microsatellite (inframe_deletion) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_deletion) | Axenfeld-Rieger syndrome type 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |