ClinVar Miner

Variants studied for Dilated cardiomyopathy 1JJ

Coded as:
Minimum submission review status: Collection method:
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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 0 673 414 89 1144

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance likely benign benign total
LAMA4 1 647 395 88 1099
LAMA4, LOC126859766 1 26 19 1 45

Submitter and significance breakdown #

Total submitters: 18
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Submitter pathogenic uncertain significance likely benign benign total
Invitae 0 650 386 84 1120
Fulgent Genetics, Fulgent Genetics 0 106 19 2 127
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 5 13 21 39
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 4 24 9 37
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 0 1 6 11 18
Genome-Nilou Lab 0 0 0 12 12
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 1 1 6 8
Revvity Omics, Revvity Omics 0 6 0 0 6
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine 0 4 0 0 4
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 3 0 0 3
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 3 0 0 3
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 3 0 0 3
OMIM 2 0 0 0 2
Baylor Genetics 0 2 0 0 2
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 1 2
Mendelics 0 0 0 1 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 1 0 0 1
Phosphorus, Inc. 0 1 0 0 1

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