Disorders

Short QT Syndrome 1

Synonym(s): SQT1

Gene	Locus	Protein
KCNH2	7q36.1	Potassium voltage-gated channel subfamily H member 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
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany
Maastricht University Medical Centre, Clinical Genomics - Maastricht, Netherlands
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
Seoul National University Hospital, Molecular Diagnostics Laboratory - Seoul, South Korea
Synlab MVZ Humane Genetik Mnchen, Labor fr Humangenetik - München, Germany
University Hospital Münster, Institute for Genetics of Heart Diseases (IfGH) - Münster, Germany

^* 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.