| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Hereditary angioneurotic edema +5 more | |
| | | Single nucleotide variant (intron variant) | Hereditary angioedema type 3 +1 more | |
| | | Deletion (intron variant) | Hereditary angioedema type 3 +1 more | |
| | | Single nucleotide variant (missense variant) | Factor XII deficiency disease +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified +3 more | |
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