ClinVar Miner

Variants studied for dilated cardiomyopathy 1D

Included ClinVar conditions (3):
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
21 6 89 27 7 149

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
TNNT2 21 6 89 27 7 149

Submitter and significance breakdown #

Total submitters: 11
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 16 5 84 27 7 139
OMIM 7 0 0 0 0 7
Human Genome Sequencing Center Clinical Lab,Baylor College of Medicine 2 0 0 0 0 2
Center for Medical Genetics Ghent,University of Ghent 1 0 1 0 0 2
Center of Genomic medicine, Geneva,University Hospital of Geneva 0 0 2 0 0 2
Equipe Genetique des Anomalies du Developpement,Université de Bourgogne 0 0 2 0 0 2
Fulgent Genetics,Fulgent Genetics 0 1 0 0 0 1
Illumina Clinical Services Laboratory,Illumina 0 0 1 0 0 1
Knight Diagnostic Laboratories,Oregon Health and Sciences University 0 0 1 0 0 1
Petrovsky Russian Research Center of Surgery, The Federal Agency for Scientific Organizations 1 0 0 0 0 1
Phosphorus, Inc. 0 0 1 0 0 1

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