ClinVar Miner

Variants studied for arrhythmogenic right ventricular dysplasia 2

Included ClinVar conditions (2):
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 2 220 49 33 306

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 2 220 49 33 306

Submitter and significance breakdown #

Total submitters: 11
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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
Fulgent Genetics,Fulgent Genetics 1 0 13 0 0 14
Division of Human Genetics,Children's Hospital of Philadelphia 0 0 4 0 0 4
OMIM 2 0 0 0 0 2
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 2 0 0 2
Phosphorus, Inc. 0 0 2 0 0 2
Baylor Genetics 1 0 0 0 0 1
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 0 0 1 0 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 0 1 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 0 0 1
Johns Hopkins Genomics,Johns Hopkins University 0 1 0 0 0 1

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