| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Cone-rod dystrophy 13 +2 more | |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 13 | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis 6 +2 more | GPathogenic/Likely pathogenic |
| | ARHGEF40, BCL2L2
+152 more | Copy number gain | not provided | |
Click to view in NCBI Gene