| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (splice acceptor variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Factor XII deficiency disease | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
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