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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000441.2(SLC26A4):c.1708-18T>A | Benign | Pendred syndrome | 2020-03-19 | 1.0 | - | SLC26A4 |
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