| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (3 prime UTR variant) | CRYGB-related disorder | |
| | | Single nucleotide variant (synonymous variant) | CRYGB-related disorder | |
| | | Single nucleotide variant (synonymous variant) | CRYGB-related disorder +1 more | |
| | LOC100507443, CRYGB (R60H) | Single nucleotide variant (missense variant) | Cataract 39 multiple types +1 more | |
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