SLC4A3

solute carrier family 4 member 3
OMIM: 106195, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber SLC4A3 in Short QT syndrome Version 3.10 Latest signed off version: v3.1 (22 Mar 2023) Component of the following Super Panels: Cardiac arrhythmias Sudden unexplained death or survivors of a cardiac event	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber West Midlands, Oxford and Wessex GLH South West GLH Literature Phenotypes short QT ventricular fibrillation cardiac arrest

Panel

Reviews

Mode of inheritance

Details

Version 3.10
Latest signed off version: v3.1 (22 Mar 2023)

Component of the following Super Panels:

Cardiac arrhythmias

Sudden unexplained death or survivors of a cardiac event

review

MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown