| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Telangiectasia, hereditary hemorrhagic, type 2 | |
| | | Single nucleotide variant (missense variant) | Telangiectasia, hereditary hemorrhagic, type 2 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Telangiectasia, hereditary hemorrhagic, type 2 +5 more | |
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