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.594C>G (p.Pro198=) | Benign | FOXG1 disorder | 2024-07-01 | 1.0 | ClinGen Rett and Angelman-like Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for FOXG1 Version 3.0.0 | FOXG1 |
Showing 1 to 1 of 1 rows