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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000260.3(MYO7A):c.905G>A (p.Arg302His) | Likely Benign | Usher syndrome | 2019-07-17 | 1.0 | - | MYO7A |
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