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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001110792.2(MECP2):c.433C>T (p.Arg145Cys) | Pathogenic | Rett syndrome | 2022-07-25 | 2.0 | - | MECP2 |
| View | NM_001110792.2(MECP2):c.433C>T (p.Arg145Cys) | Uncertain Significance | Rett syndrome | 2022-06-28 | 1.0 | - | MECP2 |
Showing 1 to 2 of 2 rows