ClinVar Miner

Variants studied for Focal segmental glomerulosclerosis 8

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
2 0 17 4 24 1 47

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign not provided total
ANLN 2 17 4 24 1 47

Submitter and significance breakdown #

Total submitters: 14
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Submitter pathogenic uncertain significance likely benign benign not provided total
Genome-Nilou Lab 0 0 1 24 0 25
Fulgent Genetics, Fulgent Genetics 0 4 3 1 0 8
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 0 4 0 0 0 4
OMIM 2 0 0 0 0 2
Baylor Genetics 0 2 0 0 0 2
Revvity Omics, Revvity Omics 0 2 0 0 0 2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 2 0 0 0 2
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine 0 2 0 0 0 2
Institute of Human Genetics, Cologne University 0 1 0 0 0 1
Mendelics 1 0 0 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 0 0 0 0 1
GenomeConnect, ClinGen 0 0 0 0 1 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 0 1
Precision Medicine Center, Zhengzhou University 0 1 0 0 0 1

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