ClinVar Miner

Variants studied for Familial juvenile gout

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
14 6 3 0 0 23

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
UMOD 14 6 3 23

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance total
OMIM 12 0 0 12
Institute of Human Genetics,Cologne University 0 1 2 3
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 0 3 0 3
Mendelics 1 0 1 2
Institute of Human Genetics,Klinikum rechts der Isar 1 0 0 1
Center of Genomic medicine, Geneva,University Hospital of Geneva 0 1 0 1
Department of Medical Genetics,Sanjay Gandhi Post Graduate Institute of Medical Sciences 0 1 0 1

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