ClinVar Miner

Variants studied for Arrhythmogenic right ventricular dysplasia 10

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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 not provided total
107 63 868 527 48 1 1541

Gene and significance breakdown #

Total genes and gene combinations: 6
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
DSG2 101 55 833 504 47 0 1474
DSG2, LOC130062340 5 6 30 23 1 0 60
DSG2, TTR 0 0 4 0 0 0 4
DSC2, DSG2 0 1 1 0 0 1 1
DYNC2H1 1 0 0 0 0 0 1
PRKAR1A 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 38
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 98 25 789 499 44 0 1455
Illumina Laboratory Services, Illumina 0 1 92 31 11 0 135
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 4 1 10 1 0 0 16
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 2 7 0 0 0 0 9
OMIM 9 0 0 0 0 0 9
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 3 4 0 0 0 7
Institute of Human Genetics, University of Leipzig Medical Center 1 4 1 0 0 0 6
Variantyx, Inc. 2 4 0 0 0 0 6
KardioGenetik, Herz- und Diabeteszentrum NRW 0 2 3 0 0 0 5
3billion 2 2 0 0 0 0 4
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 1 1 1 1 0 0 4
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 1 2 0 0 0 3
Baylor Genetics 1 1 0 0 0 0 2
Clinical Genomics Laboratory, Stanford Medicine 0 0 2 0 0 0 2
Clinical Genomics Laboratory, Washington University in St. Louis 0 2 0 0 0 0 2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 1 0 1 0 0 0 2
Human Genetics Bochum, Ruhr University Bochum 1 0 1 0 0 0 2
Medical Genome Center, National Cerebral and Cardiovascular Center 1 0 1 0 0 0 2
Mendelics 2 0 0 0 0 0 2
Breda Genetics srl, Breda Genetics srl 0 1 0 0 0 0 1
CENTOGENE GmbH and LLC - Guiding Precision Medicine 0 1 0 0 0 0 1
Center for Human Genetics and Genomic Medicine, Uniklinik Rwth Aachen 0 1 0 0 0 0 1
Department of Human Genetics, Hannover Medical School 1 0 0 0 0 0 1
Division of Medical Genetics, University of Washington 0 1 0 0 0 0 1
Genetics and Molecular Pathology, SA Pathology 1 0 0 0 0 0 1
GenomeConnect, ClinGen 0 0 0 0 0 1 1
Genomics England Pilot Project, Genomics England 0 1 0 0 0 0 1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 0 1 0 0 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 0 0 0 0 0 1
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 0 1 0 0 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 1 0 0 0 0 0 1
Juno Genomics, Hangzhou Juno Genomics, Inc 0 1 0 0 0 0 1
MGZ Medical Genetics Center 0 1 0 0 0 0 1
MVZ Martinsried, Medicover Genetics 0 0 1 0 0 0 1
MVZ Medizinische Genetik Mainz 0 1 0 0 0 0 1
OLLIN Analises Genomicas, OLLIN 0 1 0 0 0 0 1
Petrovsky National Research Centre of Surgery, The Federal Agency for Scientific Organizations 0 1 0 0 0 0 1
Phosphorus, Inc. 0 0 1 0 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. The submitted information has not been verified. If you have questions about the information contained on this website, please see a health care professional.