ClinVar Miner

Variants studied for Dilated cardiomyopathy 1DD

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
13 14 972 814 106 1765

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
RBM20 12 14 963 814 106 1755
TNNT2 1 0 4 0 0 5
BBIP1, PDCD4, RBM20, SHOC2 0 0 2 0 0 2
LOC130004734, RBM20 0 0 2 0 0 2
LOC111875823, LOC126861041, LOC130004733, LOC130004734, RBM20 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 40
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Labcorp Genetics (formerly Invitae), Labcorp 9 3 767 787 93 1659
Illumina Laboratory Services, Illumina 0 0 128 16 12 156
Fulgent Genetics, Fulgent Genetics 2 0 110 8 0 120
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 12 9 11 32
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 3 20 5 28
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 1 2 7 1 0 11
Revvity Omics, Revvity 1 0 6 0 0 7
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 7 0 0 7
OMIM 6 0 0 0 0 6
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 6 0 0 6
Evolutionary and Medical Genetics Laboratory, Centre for Cellular and Molecular Biology 1 0 4 0 0 5
Clinical Genomics Laboratory, Stanford Medicine 0 0 5 0 0 5
Genome-Nilou Lab 0 0 0 0 5 5
Mendelics 0 0 1 1 2 4
Baylor Genetics 1 2 0 0 0 3
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues 0 2 1 0 0 3
Division of Human Genetics, Children's Hospital of Philadelphia 0 0 2 0 0 2
Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine 0 0 2 0 0 2
Petrovsky National Research Centre of Surgery, The Federal Agency for Scientific Organizations 0 1 1 0 0 2
Centre for Mendelian Genomics, University Medical Centre Ljubljana 1 0 1 0 0 2
Institute of Human Genetics, University of Goettingen 0 1 0 0 0 1
North West Genomic Laboratory Hub, Manchester University NHS Foundation Trust 1 0 0 0 0 1
Mayo Clinic Laboratories, Mayo Clinic 0 0 1 0 0 1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 1 0 0 1
Center for Medical Genetics Ghent, University of Ghent 0 1 0 0 0 1
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute 0 1 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 1 0 0 1
Center for Human Genetics, University of Leuven 1 0 0 0 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 1 0 0 0 0 1
Juno Genomics, Hangzhou Juno Genomics, Inc 0 1 0 0 0 1
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital 1 0 0 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 0 1
3billion 1 0 0 0 0 1
KTest Genetics, KTest 1 0 0 0 0 1
Clinical Center for Gene Diagnosis and Therapy, Department of Cardiovascular Surgery, The Second Xiangya Hospital of Central South University 0 0 1 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 0 1 0 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 0 0 1 0 0 1
KardioGenetik, Herz- und Diabeteszentrum NRW 0 0 1 0 0 1
MVZ Medizinische Genetik Mainz 0 0 1 0 0 1

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