|Short QT syndrome v1.4||SCN3B||James Eden reviewed gene: SCN3B: Rating: RED; Mode of pathogenicity: ; Publications: 19862833, 30420954, 16301704; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Current diagnostic: yes|
|Short QT syndrome v1.3||SCN3B||
Ellen McDonagh Source North West GLH was added to SCN3B.
Publications for gene SCN3B were changed from to 30420954; 19862833; 16301704
|Short QT syndrome v0.2||SCN3B||
Sarah Leigh gene: SCN3B was added
gene: SCN3B was added to Short QT syndrome. Sources: Brugada syndrome (Version 1.7)
Mode of inheritance for gene: SCN3B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown