| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CRYGD, LOC100507443 (G61C) | Single nucleotide variant (missense variant) | Aculeiform cataract +1 more | GConflicting classifications of pathogenicity |
| | CRYGC, LOC100507443 (R168W) | Single nucleotide variant (missense variant) | Cataract 2, multiple types +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Cataract 39 multiple types +1 more | |
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