Showing 1 to 3 of 3 rows
See Report
Preferred Variant Title
Classification
Condition
Published Date
Version
Criteria Specification
Gene
View NM_001110792.2(MECP2):c.379C>T (p.Arg127Cys)
Uncertain Significance
Rett syndrome2023-09-15
2.1
-MECP2
View NM_001110792.2(MECP2):c.379C>T (p.Arg127Cys)
Uncertain Significance
Rett syndrome2023-08-24
2.0
-MECP2
View NM_001110792.2(MECP2):c.379C>T (p.Arg127Cys)
Uncertain Significance
Rett syndrome2021-12-27
1.0
-MECP2
Showing 1 to 3 of 3 rows