ClinVar Miner

Variants studied for Dilated cardiomyopathy 1C

Coded as:
Minimum submission review status: Collection method:
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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
10 2 55 5 5 77

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
LDB3 8 2 46 5 2 63
LDB3, LOC110121486 2 0 7 0 3 12
LDB3, LOC130004243 0 0 1 0 0 1
RYR2 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 18
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 21 1 3 25
Cytogenetics- Mohapatra Lab, Banaras Hindu University 4 2 12 3 3 24
OMIM 5 0 1 0 0 6
Baylor Genetics 0 0 5 0 0 5
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 2 1 0 3
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 3 0 0 3
New York Genome Center 0 0 3 0 0 3
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute 0 0 2 0 0 2
Centogene AG - the Rare Disease Company 0 0 1 0 0 1
Mendelics 1 0 0 0 0 1
Center of Genomic medicine, Geneva, University Hospital of Geneva 0 0 1 0 0 1
Genetics and Molecular Pathology, SA Pathology 0 0 1 0 0 1
Breda Genetics srl 0 0 1 0 0 1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 0 1 0 0 1
Genome-Nilou Lab 0 0 0 0 1 1
Institute of Immunology and Genetics Kaiserslautern 0 0 1 0 0 1
KardioGenetik, Herz- und Diabeteszentrum NRW 0 0 1 0 0 1
Regional Center For Medical Genetics Timis, Louis Turcanu Emergency Hospital for Children Timisoara 0 0 1 0 0 1

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