| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CASP7, LOC126861046 (V171I +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CASP7, LOC126861046 (L105F +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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