ClinVar Miner

Variants studied for dilated cardiomyopathy 1DD

Included ClinVar conditions (1):
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
8 4 202 80 24 305

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
RBM20 7 4 197 80 24 299
TNNT2 1 0 4 0 0 5
LOC111875823, RBM20 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 14
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 5 1 191 65 20 282
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen 0 1 5 20 5 31
Fulgent Genetics,Fulgent Genetics 2 0 5 0 0 7
OMIM 6 0 0 0 0 6
Evolutionary and Medical Genetics Laboratory, Centre for Cellular and Molecular Biology 1 0 4 0 0 5
Division of Human Genetics,Children's Hospital of Philadelphia 0 0 2 0 0 2
Baylor-Hopkins Center for Mendelian Genomics,Johns Hopkins University 0 0 2 0 0 2
Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues 0 1 1 0 0 2
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 0 0 1 0 0 1
Illumina Clinical Services Laboratory,Illumina 0 0 1 0 0 1
Center for Medical Genetics Ghent,University of Ghent 0 1 0 0 0 1
Knight Diagnostic Laboratories,Oregon Health and Sciences University 0 0 1 0 0 1
Center for Human Genetics,University of Leuven 1 0 0 0 0 1
Petrovsky Russian Research Center of Surgery, The Federal Agency for Scientific Organizations 0 0 1 0 0 1

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