Short QT syndromeGene: SCN3B
Gene currently tested by alternative panel, very few short QT referrals to date. Only class 1-3 variants detected in this gene. 7 variants listed on HGMD (accessed 29/01/2019). ClinGen Knowledge Base: disputed association with Brugada syndrome (accessed 29/01/2019).
Created: 14 Feb 2019, 1:38 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Variants in this GENE are reported as part of current diagnostic practice
Source North West GLH was added to SCN3B. Publications for gene SCN3B were changed from to 30420954; 19862833; 16301704
Jules Hancox: This is a very recent report.
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