ClinVar Miner

Variants studied for Arrhythmogenic right ventricular cardiomyopathy, type 11

Coded as:
Minimum submission review status: Collection method:
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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
17 10 249 74 25 348

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
DSC2 15 8 235 71 24 326
DSC2, DSCAS 2 2 14 3 1 22

Submitter and significance breakdown #

Total submitters: 15
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 14 7 170 58 17 266
Illumina Clinical Services Laboratory,Illumina 0 0 82 11 9 102
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center 1 0 4 8 8 21
Genome Diagnostics Laboratory,University Medical Center Utrecht 2 0 1 7 6 16
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen 0 2 2 5 6 15
OMIM 2 0 1 0 0 3
Mendelics 0 0 1 0 1 2
Fulgent Genetics,Fulgent Genetics 0 0 2 0 0 2
Phosphorus, Inc. 0 0 2 0 0 2
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 0 1 0 0 0 1
Division of Human Genetics,Children's Hospital of Philadelphia 0 0 1 0 0 1
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City 0 0 1 0 0 1
Department of Medical Bioinformatics,Sinopath Diagnosis 0 1 0 0 0 1
Department of Genetics,Sultan Qaboos University Hospital, Oman 0 0 1 0 0 1
UNC Molecular Genetics Laboratory,University of North Carolina at Chapel Hill 0 1 0 0 0 1

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