Short QT syndromeGene: SNTA1
Gene currently tested by alternative panel, very few short QT referrals to date. 18 variants listed on HGMD (accessed 29/01/2019). ClinGen Knowledge Base: gene not curated (accessed 29/01/2019).
Created: 14 Feb 2019, 1:38 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Long QT syndrome 12 (612955)
Variants in this GENE are reported as part of current diagnostic practice
Source North West GLH was added to SNTA1. Added phenotypes Long QT syndrome 12 (612955) for gene: SNTA1 Publications for gene SNTA1 were changed from to 30420954; 19862833; 16301704
Jules Hancox: This is a very recent report.
gene: SNTA1 was added gene: SNTA1 was added to Short QT syndrome. Sources: Long QT syndrome (Version 1.5),Emory Genetics Laboratory Mode of inheritance for gene: SNTA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted