ClinVar Miner

Variants studied for Beck-Fahrner syndrome

Included ClinVar conditions (1):
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 total
16 20 76 3 3 114

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
TET3 16 20 76 3 3 114

Submitter and significance breakdown #

Total submitters: 38
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center 0 1 11 0 0 12
New York Genome Center 0 0 10 0 0 10
OMIM 9 0 0 0 0 9
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 4 0 4 0 0 8
Revvity Omics, Revvity 0 0 7 0 0 7
Institute of Human Genetics, University of Leipzig Medical Center 0 3 3 0 0 6
Fulgent Genetics, Fulgent Genetics 0 0 3 2 0 5
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 5 0 0 5
Illumina Laboratory Services, Illumina 0 0 5 0 0 5
Neuberg Centre For Genomic Medicine, NCGM 0 0 5 0 0 5
Clinical Genomics Laboratory, Washington University in St. Louis 0 1 3 0 0 4
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 4 0 0 4
3billion 1 1 1 0 0 3
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 0 3 0 0 0 3
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 3 0 0 3
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 2 0 1 0 3
Genome-Nilou Lab 0 0 0 0 3 3
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 0 1 2 0 0 3
Baylor Genetics 0 0 2 0 0 2
Institute of Human Genetics, University Hospital of Duesseldorf 0 0 2 0 0 2
Laboratoire Génétique Moléculaire, CHRU TOURS 0 0 2 0 0 2
MGZ Medical Genetics Center 0 1 1 0 0 2
Molecular Genetics, Royal Melbourne Hospital 0 0 2 0 0 2
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 1 0 0 1
Centre of Medical Genetics, University Hospital Muenster 0 1 0 0 0 1
Daryl Scott Lab, Baylor College of Medicine 0 1 0 0 0 1
Department of Human Genetics, University Hospital Bern, Inselspital 1 0 0 0 0 1
Department of Neurodegenerative Diseases, AG Gasser, Hertie Institute for Clinical Brain Research 0 1 0 0 0 1
Genesolutions, Medical Genetics Institutes, Ho Chi Minh City, Vietnam 0 0 1 0 0 1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 0 1 0 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 0 0 1 0 0 1
MVZ Martinsried, Medicover Genetics 0 1 0 0 0 1
MVZ Medizinische Genetik Mainz 0 1 0 0 0 1
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals 1 0 0 0 0 1
Ozbek Human Genetics Laboratory, Izmir Biomedicine and Genome Center 0 1 0 0 0 1
SIB Swiss Institute of Bioinformatics 0 0 1 0 0 1
University of Washington Department of Laboratory Medicine, University of Washington 0 0 1 0 0 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 0 0 0 0 1

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