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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_016239.4(MYO15A):c.1582G>A (p.Gly528Ser) | Likely Benign | nonsyndromic genetic deafness | 2022-05-13 | 1.0 | - | MYO15A |
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