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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000257.3(MYH7):c.5704G>C (p.Glu1902Gln) | Likely Benign | cardiomyopathy | 2021-08-25 | 1.0 | - | MYH7 |
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