Disorders

Brugada Syndrome 3

Gene	Locus	Protein
CACNA1C	12p13.3	Voltage-dependent L-type calcium channel subunit alpha-1C

Laboratory	Test Method	Prenatal	Carrier *
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany
Centogene AG, Rare Disease Company - Rostock, Germany
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA
GeneDx - Gaithersburg, MD, USA
Health in Code S.L. - A Coruña, Spain
InVitae Corporation - San Francisco, CA, USA
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain
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.