ClinVar Miner

Variants studied for Arrhythmogenic right ventricular dysplasia, familial, 2

Coded as:
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 total
4 4 204 50 33 292

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
RYR2 4 4 204 50 33 292

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 0 198 49 33 280
Institute of Human Genetics, University of Leipzig Medical Center 1 2 2 1 0 6
OMIM 2 0 0 0 0 2
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 2 0 0 2
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 1 1 0 0 2
Phosphorus, Inc. 0 0 2 0 0 2
Baylor Genetics 1 0 0 0 0 1
Division of Human Genetics,Children's Hospital of Philadelphia 0 0 1 0 0 1
Johns Hopkins Genomics,Johns Hopkins University 0 1 0 0 0 1

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