| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CRY2, LOC121832791 (R171C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CRY2, LOC121832791 (E200K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CRY2, LOC121832791 (L163I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CRY2, LOC121832791 (E245K +1 more) | Single nucleotide variant (missense variant) | not specified | |
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