SLC4A3

solute carrier family 4 member 3
OMIM: 106195, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber SLC4A3 in Short QT syndrome Level 2: Cardiology Version 3.22 Latest signed off version: v3.16 (6 May 2026) Component of the following Super Panels: Cardiac arrhythmias Sudden unexplained death or survivors of a cardiac event Unexplained death in infancy and sudden unexplained death in childhood	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber West Midlands, Oxford and Wessex GLH South West GLH Literature Phenotypes Short QT syndrome 7, OMIM:620231 short QT syndrome 7, MONDO:0859368 Tags Q2_26_promote_green

Panel

Reviews

Mode of inheritance

Details

Level 2: Cardiology
Version 3.22
Latest signed off version: v3.16 (6 May 2026)

Component of the following Super Panels:

Cardiac arrhythmias

Sudden unexplained death or survivors of a cardiac event

Unexplained death in infancy and sudden unexplained death in childhood

review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted