ClinVar Miner

Variants studied for dilated cardiomyopathy 1D

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
44 56 349 265 36 697

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
TNNT2 44 56 349 265 36 697

Submitter and significance breakdown #

Total submitters: 35
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Labcorp Genetics (formerly Invitae), Labcorp 40 26 312 252 21 651
Genome-Nilou Lab 7 18 100 61 26 212
Fulgent Genetics, Fulgent Genetics 4 3 25 5 1 38
Illumina Laboratory Services, Illumina 0 0 12 1 0 13
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 2 2 6 1 0 11
OMIM 7 0 0 0 0 7
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 2 2 1 0 0 5
New York Genome Center 1 2 2 0 0 5
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 4 0 0 4
Institute of Human Genetics, University of Leipzig Medical Center 0 1 3 0 0 4
Juno Genomics, Hangzhou Juno Genomics, Inc 0 2 1 0 0 3
Neuberg Centre For Genomic Medicine, NCGM 2 0 1 0 0 3
Baylor Genetics 0 1 1 0 0 2
Center for Medical Genetics Ghent, University of Ghent 1 0 1 0 0 2
Center of Genomic medicine, Geneva, University Hospital of Geneva 0 0 2 0 0 2
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 0 2 0 0 2
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 0 2 0 0 0 2
KTest Genetics, KTest 2 0 0 0 0 2
Institute of Immunology and Genetics Kaiserslautern 0 0 2 0 0 2
Centogene AG - the Rare Disease Company 1 0 0 0 0 1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 1 0 0 0 1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 0 1 0 0 0 1
Stanford Center for Inherited Cardiovascular Disease, Stanford University 0 1 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 1
Petrovsky National Research Centre of Surgery, The Federal Agency for Scientific Organizations 1 0 0 0 0 1
Phosphorus, Inc. 0 0 1 0 0 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 0 1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 0 1 0 0 1
Clinical Genomics Laboratory, Stanford Medicine 0 0 1 0 0 1
3billion, Medical Genetics 0 0 1 0 0 1
Human Genetics Bochum, Ruhr University Bochum 0 0 1 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 1 0 0 0 1
Arcensus 0 1 0 0 0 1
KardioGenetik, Herz- und Diabeteszentrum NRW 0 0 1 0 0 1

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