ClinVar Miner

Variants studied for Arrhythmogenic right ventricular cardiomyopathy, type 10

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
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
28 11 274 93 42 409

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
DSG2 28 11 273 93 42 408
DSG2, TTR 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 19 8 200 65 32 324
Illumina Clinical Services Laboratory,Illumina 0 0 92 31 11 134
OMIM 9 0 0 0 0 9
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 1 3 0 0 0 4
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 1 0 2 1 0 4
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 0 1
Phosphorus, Inc. 0 0 1 0 0 1

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