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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000138.5(FBN1):c.3422C>T (p.Pro1141Leu) | Benign | Marfan syndrome | 2022-12-01 | 1.0 | - | FBN1 |
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