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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000138.5(FBN1):c.1481G>C (p.Cys494Ser) | Likely Pathogenic | Marfan syndrome | 2023-11-16 | 1.0 | ClinGen FBN1 Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1 | FBN1 |
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