ClinVar Miner

Variants studied for Vesicoureteral reflux 2

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
2 0 74 32 77 174

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance likely benign benign total
ROBO2 2 70 31 75 167
LOC126806727, ROBO2 0 4 1 2 7

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 61 18 74 153
Fulgent Genetics, Fulgent Genetics 0 6 16 1 23
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 3 0 0 3
OMIM 2 0 0 0 2
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 0 0 2 2
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 2 2
Baylor Genetics 0 1 0 0 1
Revvity Omics, Revvity Omics 0 1 0 0 1
Mendelics 0 0 0 1 1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 1 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 1 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 0 1
Human Genetic Laboratory, University of Liege 0 1 0 0 1

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