Disorders


 

TNNC1-Related Familial Hypertrophic Cardiomyopathy


 

OMIM

GeneLocusProtein
TNNC13p21.1Troponin C, slow skeletal and cardiac muscles

Laboratory Test Method Prenatal Carrier *
Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA  
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  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
Transgenomic - New Haven, CT, USA  

* 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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