ClinVar Miner

Variants studied for primary membranoproliferative glomerulonephritis

Included ClinVar conditions (9):
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 risk factor total
24 28 289 51 39 5 426

Gene and significance breakdown #

Total genes and gene combinations: 6
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
CFH 11 18 182 39 35 0 276
CFHR5 2 0 94 6 0 0 102
DGKE 11 8 13 6 3 5 45
C3 0 1 0 0 0 0 1
CFH, KCNT2 0 1 0 0 0 0 1
CFHR2 0 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 26
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
Fulgent Genetics, Fulgent Genetics 8 15 243 41 6 0 313
Genome-Nilou Lab 2 4 67 28 37 0 138
OMIM 12 0 0 0 0 5 17
Neuberg Centre For Genomic Medicine, NCGM 0 1 10 0 0 0 11
Baylor Genetics 1 0 6 0 0 0 7
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 4 3 0 0 0 0 7
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 4 1 0 0 0 5
Illumina Laboratory Services, Illumina 0 0 3 1 0 0 4
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 3 0 0 0 3
MVZ Medizinische Genetik Mainz 0 0 3 0 0 0 3
NIHR Bioresource Rare Diseases, University of Cambridge 0 2 0 0 0 0 2
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 2 0 0 0 0 2
3billion, Medical Genetics 0 0 2 0 0 0 2
Molecular Genetics, Royal Melbourne Hospital 0 0 0 1 1 0 2
Revvity Omics, Revvity 0 0 1 0 0 0 1
Institute of Human Genetics, Cologne University 0 1 0 0 0 0 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 0 0 0 0 0 1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 1 0 0 0 1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 1 0 0 0 0 0 1
Clinical Genomics Laboratory, Washington University in St. Louis 0 1 0 0 0 0 1
GenePathDx, GenePath diagnostics 0 1 0 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 1 0 0 0 0 0 1
Center for Precision Medicine, Vanderbilt University Medical Center 1 0 0 0 0 0 1
Cavalleri Lab, Royal College of Surgeons in Ireland 1 0 0 0 0 0 1
Beijing Key Laboratry for Genetics of Birth Defects, Beijing Children's Hospital 0 1 0 0 0 0 1
John Atkinson Laboratory, Washington University School of Medicine in St. Louis 0 0 1 0 0 0 1

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