ClinVar Miner

Variants in gene RANBP2

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Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

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 risk factor total
3 4 344 177 69 3 572

Condition and significance breakdown #

Total conditions: 3
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Condition pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
Encephalopathy, acute, infection-induced, 3, suceptibility to 3 2 333 128 60 3 522
not provided 0 2 16 41 1 0 58
not specified 0 0 0 29 26 0 55

Submitter and significance breakdown #

Total submitters: 16
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
Invitae 1 0 327 146 60 0 534
GeneDx 0 1 11 32 26 0 70
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics 0 0 2 3 1 0 6
CeGaT Praxis fuer Humangenetik Tuebingen 0 0 3 2 0 0 5
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 1 0 0 2 1 0 4
OMIM 0 0 0 0 0 3 3
Baylor Genetics 0 0 3 0 0 0 3
GeneReviews 3 0 0 0 0 0 3
Kamineni Academy of Medical Sciences & Research Centre, Kamineni Hospitals 0 2 0 0 0 0 2
TIDEX, University of British Columbia 0 0 2 0 0 0 2
Mendelics 1 0 0 0 0 0 1
Fulgent Genetics,Fulgent Genetics 1 0 0 0 0 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 0 1
Division of Human Genetics,Children's Hospital of Philadelphia 0 0 1 0 0 0 1
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 0 1 0 0 0 1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 0 1 0 0 0 0 1

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