ClinVar Miner

Variants studied for Arrhythmogenic right ventricular dysplasia 10; Dilated cardiomyopathy 1BB

Coded as:
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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
4 12 77 14 3 108

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 4 12 75 13 3 105
DSG2, LOC130062340 0 0 2 1 0 3

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Fulgent Genetics, Fulgent Genetics 3 8 73 14 3 101
Juno Genomics, Hangzhou Juno Genomics, Inc 0 4 0 0 0 4
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 3 0 0 3
New York Genome Center 0 1 1 0 0 2
Division of Human Genetics, Children's Hospital of Philadelphia 0 0 1 0 0 1
Donald Williams Parsons Laboratory, Baylor College of Medicine 1 0 0 0 0 1

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