ClinVar Miner

Variants studied for Dilated cardiomyopathy 1DD

Coded as:
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
13 9 817 715 101 1511

Gene and significance breakdown #

Total genes and gene combinations: 5
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
RBM20 12 9 808 715 101 1501
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: 31
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 9 3 623 689 88 1412
Illumina Laboratory Services, Illumina 0 0 129 16 12 157
Fulgent Genetics, Fulgent Genetics 2 0 105 8 0 115
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 3 20 5 28
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 9 7 10 26
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 1 0 6 1 0 8
Revvity Omics, Revvity 1 0 6 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
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
Clinical Genomics Program, Stanford Medicine 0 0 3 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
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
Mayo Clinic Laboratories, Mayo Clinic 0 0 1 0 0 1
Center for Medical Genetics Ghent, University of Ghent 0 1 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 1
Center for Human Genetics, University of Leuven 1 0 0 0 0 1
Petrovsky National Research Centre of Surgery, The Federal Agency for Scientific Organizations 0 0 1 0 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 1 0 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
KardioGenetik, Herz- und Diabeteszentrum NRW 0 0 1 0 0 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.