| | | Single nucleotide variant (nonsense +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | CABP4-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (intron variant) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | Cone-rod synaptic disorder, congenital nonprogressive +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +4 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (missense variant) | Cone-rod synaptic disorder, congenital nonprogressive +1 more | |
| | | Single nucleotide variant (missense variant) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Deletion (5 prime UTR variant +3 more) | Cone-rod synaptic disorder, congenital nonprogressive +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | Cone-rod synaptic disorder, congenital nonprogressive +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Indel (5 prime UTR variant +3 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (nonsense +1 more) | Retinal dystrophy +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Cone-rod synaptic disorder, congenital nonprogressive +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (synonymous variant) | Cone-rod synaptic disorder, congenital nonprogressive +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cone-rod synaptic disorder, congenital nonprogressive | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Cone-rod synaptic disorder, congenital nonprogressive +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |