Disorders


 

Long QT Syndrome 12


Synonym(s): LQT 12, LQT12

 

OMIM

GeneLocusProtein
SNTA120q11.2 

Laboratory Test Method Prenatal Carrier *
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany  
Centogene AG, Rare Disease Company - Rostock, Germany  
GeneDx - Gaithersburg, MD, USA  
InVitae Corporation - San Francisco, CA, USA  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
Transgenomic - New Haven, CT, USA  
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.

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