| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CES2, LOC126862376 (N183I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CES2, LOC126862376 (N250K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CES2, LOC126862376 (M261I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CES2, LOC126862376 (S414C +1 more) | Single nucleotide variant (missense variant) | not specified | |
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