Disorders

MYL3-Related Familial Hypertrophic Cardiomyopathy

Gene	Locus	Protein
MYL3	3p	Myosin light chain 3

Laboratory	Test Method	Prenatal	Carrier *
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands
Centogene AG, Rare Disease Company - Rostock, Germany
Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA
Correlagen Diagnostics, Inc. - Westborough, MA, USA
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany
GeneDx - Gaithersburg, MD, USA
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA
Health in Code S.L. - A Coruña, Spain
InVitae Corporation - San Francisco, CA, USA
Maastricht University Medical Centre, Clinical Genomics - Maastricht, Netherlands
Oslo University Hospital HF - Ullevaal, Department of Medical Genetics - Unit for Cardiac and Cardiavasular Genetics - Oslo, Norway
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, Great Britain
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
Transgenomic - New Haven, CT, USA
University of Goettingen, Institute of Human Genetics - Goettingen, 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.