ClinVar Miner

Variants studied for Peroxisome biogenesis disorder 9B

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 total
60 31 163 285 24 545

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
PEX7 60 31 163 285 24 545

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 58 12 140 279 17 506
Baylor Genetics 16 21 1 0 0 38
Illumina Laboratory Services, Illumina 0 0 28 5 4 37
OMIM 7 0 0 0 0 7
Genome-Nilou Lab 0 0 1 1 4 6
Centre for Mendelian Genomics, University Medical Centre Ljubljana 2 0 0 0 0 2
Institute of Human Genetics, University of Goettingen 0 0 1 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 1 0 0 0 0 1

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