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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_002693.2(POLG):c.3293A>C (p.Asn1098Thr) | Uncertain Significance | mitochondrial disease | 2021-05-07 | 1.0 | - | POLG |
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