| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CASP2, LOC129999515 (A19T) | Single nucleotide variant (missense variant) | CASP2-related disorder | |
| | | Single nucleotide variant (missense variant) | CASP2-related disorder | |
| | | Single nucleotide variant (intron variant) | CASP2-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | CASP2-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | CASP2-related disorder | |
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