ClinVar Miner

Variants studied for C3 glomerulonephritis

Included ClinVar conditions (1):
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
4 0 25 17 14 52

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign total
CFHR5 4 25 17 14 52

Submitter and significance breakdown #

Total submitters: 15
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Submitter pathogenic uncertain significance likely benign benign total
Genome-Nilou Lab 0 17 13 12 42
Fulgent Genetics, Fulgent Genetics 0 10 9 2 21
Revvity Omics, Revvity 0 4 0 0 4
OMIM 2 0 0 0 2
Baylor Genetics 0 2 0 0 2
Institute of Human Genetics, University of Leipzig Medical Center 0 2 0 0 2
Centogene AG - the Rare Disease Company 0 1 0 0 1
Mendelics 0 0 0 1 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 0 0 0 1
Center of Genomic medicine, Geneva, University Hospital of Geneva 1 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 1 0 0 1
Genetics and Molecular Pathology, SA Pathology 0 1 0 0 1
Al Jalila Children's Genomics Center, Al Jalila Childrens Speciality Hospital 0 1 0 0 1
New York Genome Center 0 1 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 1 0 0 1

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