If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one
conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of
the conflicted variants cells to its left.
Variants with only 1 submission
per condition
Variants with at least 2 submissions
on the same condition
and no conflicts
Variants with a synonymous conflict (e.g. benign vs non-pathogenic)
Variants with a confidence conflict (e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict
Variants with a category conflict (e.g. benign vs affects)
Variants with a clinically significant conflict (e.g. benign vs pathogenic)
Variants with any conflict
143
45
0
35
0
0
8
43
Significance breakdown #
In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e.
variants that have been annotated with different terms that map to the same standard term. To compare the terms
that were actually submitted, check the box in the filters section at the top of this page.
Submitter to submitter summary #
Submitter
Variants with only 1 submission
per condition
Variants with at least 2 submissions
on the same condition
and no conflicts
Variants with a synonymous conflict (e.g. benign vs non-pathogenic)
Variants with a confidence conflict (e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict
Variants with a category conflict (e.g. benign vs affects)
Variants with a clinically significant conflict (e.g. benign vs pathogenic)
Variants with any conflict
Labcorp Genetics (formerly Invitae), Labcorp
0
14
0
13
0
0
3
16
Baylor Genetics
0
16
0
8
0
0
0
8
Women's Health and Genetics/Laboratory Corporation of America, LabCorp
0
11
0
7
0
0
0
7
Fulgent Genetics, Fulgent Genetics
0
6
0
5
0
0
0
5
Natera, Inc.
0
10
0
5
0
0
0
5
Department of Medical Genetics, International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine
0
0
0
4
0
0
0
4
Genome-Nilou Lab
0
2
0
2
0
0
2
4
Juno Genomics, Hangzhou Juno Genomics, Inc
0
3
0
4
0
0
0
4
3billion
0
12
0
3
0
0
0
3
ClinGen PAH Variant Curation Expert Panel
0
5
0
3
0
0
0
3
Department of Pathology and Laboratory Medicine, Sinai Health System
0
4
0
2
0
0
1
3
OMIM
0
16
0
3
0
0
0
3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute
0
9
0
3
0
0
0
3
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City
0
0
0
2
0
0
0
2
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne
0
2
0
2
0
0
0
2
Illumina Laboratory Services, Illumina
0
4
0
2
0
0
0
2
Institute of Human Genetics, University of Leipzig Medical Center
0
5
0
2
0
0
0
2
Lifecell International Pvt. Ltd
0
1
0
2
0
0
0
2
Mendelics
0
1
0
2
0
0
0
2
Revvity Omics, Revvity
0
6
0
1
0
0
1
2
Variantyx, Inc.
0
3
0
2
0
0
0
2
Beijing Key Laboratry for Genetics of Birth Defects, Beijing Children's Hospital
0
2
0
1
0
0
0
1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare
0
0
0
1
0
0
0
1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard
0
3
0
0
0
0
1
1
CENTOGENE GmbH and LLC - Guiding Precision Medicine
0
2
0
1
0
0
0
1
Center of Excellence for Medical Genomics, Chulalongkorn University
0
0
0
1
0
0
0
1
Center of Human Genetics, Hôpital Erasme
0
0
0
1
0
0
0
1
Counsyl
0
2
0
1
0
0
0
1
Daryl Scott Lab, Baylor College of Medicine
0
2
0
1
0
0
0
1
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet
0
0
0
1
0
0
0
1
Department of Human Genetics, Hannover Medical School
0
2
0
1
0
0
0
1
Division of Genetic & Genomic Pathology, Hong Kong Children's Hospital
0
0
0
1
0
0
0
1
Dubai Health Genomic Medicine Center, Dubai Health
0
1
0
1
0
0
0
1
First Genomix Gene Laboratory, Genetic Diagnostics Department
0
1
0
1
0
0
0
1
GeneDx
0
0
0
0
0
0
1
1
Genetics and Molecular Pathology, SA Pathology
0
1
0
1
0
0
0
1
GenomeConnect - Simons Searchlight
0
4
0
1
0
0
0
1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia
0
1
0
1
0
0
0
1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre
0
4
0
1
0
0
0
1
Genomics England Pilot Project, Genomics England
0
0
0
1
0
0
0
1
Génétique des Maladies du Développement, Hospices Civils de Lyon
0
1
0
1
0
0
0
1
Human Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo
0
0
0
1
0
0
0
1
Institute of Human Genetics Munich, TUM University Hospital
0
5
0
0
0
0
1
1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen
0
1
0
1
0
0
0
1
Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital
0
1
0
1
0
0
0
1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India
0
0
0
1
0
0
0
1
Laboratoire de Génétique Moléculaire, CHU Bordeaux
0
1
0
1
0
0
0
1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein
0
3
0
1
0
0
0
1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens
0
3
0
1
0
0
0
1
MGZ Medical Genetics Center
0
2
0
1
0
0
0
1
Medical Genetic Diagnosis and Therapy Center, Fujian Medical University
0
1
0
1
0
0
0
1
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals
0
0
0
1
0
0
0
1
Neuberg Centre For Genomic Medicine, NCGM
0
3
0
1
0
0
0
1
Neurology Department, Shenzhen Children's Hospital
0
0
0
1
0
0
0
1
OLLIN Analises Genomicas, OLLIN
0
0
0
1
0
0
0
1
Pathology and Clinical Laboratory Medicine, King Fahad Medical City
0
0
0
1
0
0
0
1
Pediatric Department, Peking University First Hospital
0
0
0
1
0
0
0
1
Quest Diagnostics Nichols Institute San Juan Capistrano
0
0
0
0
0
0
1
1
SIB Swiss Institute of Bioinformatics
0
0
0
1
0
0
0
1
Solve-RD Consortium
0
0
0
1
0
0
0
1
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas
0
0
0
1
0
0
0
1
All variants with conflicting interpretations #
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.