| | CRYGD, LOC100507443 (Y56*) | Single nucleotide variant (nonsense) | Aculeiform cataract +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Joubert syndrome 17 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (splice acceptor variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (nonsense) | Orofaciodigital syndrome type 6 +2 more | |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +1 more | |
| | CPLANE1, LOC129389274 (S1487N) | Single nucleotide variant (missense variant) | Joubert syndrome 17 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +2 more | |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +2 more | |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +1 more | |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +1 more | |
| | | Single nucleotide variant (nonsense) | Joubert syndrome 17 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 17 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |