Disorders

Short QT Syndrome 3

Synonym(s): SQT3

Gene	Locus	Protein
KCNJ2	17q24.3	Inward rectifier potassium channel 2

Laboratory	Test Method	Prenatal	Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany
GeneDx - Gaithersburg, MD, USA
Health in Code S.L. - A Coruña, Spain
InVitae Corporation - San Francisco, CA, USA
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
University Hospital Münster, Institute for Genetics of Heart Diseases (IfGH) - Münster, Germany
University Hospitals of Geneva - Genetic Medicine, Genetic Oncology - DiagMol - Geneva, Switzerland

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.