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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001083962.2(TCF4):c.1990G>A (p.Ala664Thr) | Benign | Pitt-Hopkins syndrome | 2024-12-13 | 1.0 | ClinGen Rett and Angelman-like Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for TCF4 Version 3.0.0 | TCF4 |
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