| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CLSTN2, LOC126806828 (A440V) | Single nucleotide variant (missense variant) | not specified | |
| | CLSTN2, LOC126806828 (L446R) | Single nucleotide variant (missense variant) | not specified | |
| | CLSTN2, LOC126806828 (T436I) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Copy number gain | not provided | |
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