Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_001165963.4(SCN1A):c.2941C>A (p.Leu981Ile) | Uncertain Significance | generalized epilepsy with febrile seizures plus | 2024-11-05 | 1.0 | ClinGen Epilepsy Sodium Channel Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for SCN1A Version 1.0.0 | SCN1A |
Showing 1 to 1 of 1 rows