| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CIC, LOC130064572 (P1631L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CIC, LOC130064572 (A1646T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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