Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_005249.5(FOXG1):c.275C>T (p.Ala92Val) | Likely Benign | FOXG1 disorder | 2023-12-08 | 1.0 | - | FOXG1 |
Showing 1 to 1 of 1 rows