ClinVar Miner

Variants studied for Hypertrophic cardiomyopathy 15

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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
2 1 8 0 4 15

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
VCL 2 1 8 4 15

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance benign total
Genome-Nilou Lab 0 0 0 4 4
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 3 0 3
OMIM 2 0 0 0 2
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute 0 0 2 0 2
Laboratory of Genetics and Molecular Cardiology, University of São Paulo 0 1 0 0 1
Center of Genomic medicine, Geneva, University Hospital of Geneva 0 0 1 0 1
Phosphorus, Inc. 0 0 1 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 1
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 0 0 1 0 1

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