ClinVar Miner

Variants studied for Peroxisome biogenesis disorder 6A (Zellweger)

Coded as:
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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
14 32 65 6 13 128

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
PEX10 14 32 46 4 12 106
PEX10, RER1 0 0 19 2 1 22

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 1 0 59 6 11 77
Baylor Genetics 11 31 3 0 0 45
Genome-Nilou Lab 0 0 2 1 4 7
OMIM 5 0 0 0 0 5
Counsyl 2 1 0 0 0 3
Mendelics 2 0 0 0 0 2
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 1 0 0 1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 0 0 0 0 1 1
Myelin Disorders Clinic-Children's Medical Center/Medical Genetics Lab-Tarbiat Modares University, Children's Medical Center, Pediatrics Center of Excellence, 0 0 1 0 0 1

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