Variants studied for Dilated cardiomyopathy 1Z

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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
6	1	15	1	0	23

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	total
TNNC1	6	1	15	1	23

Submitter and significance breakdown #

Total submitters: 9

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	total
Illumina Laboratory Services, Illumina	0	0	10	1	11
OMIM	4	0	0	0	4
Baylor Genetics	1	0	1	0	2
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen	0	0	1	0	1
Genetics and Molecular Pathology, SA Pathology	0	0	1	0	1
The Genetics Institute, Rambam Health Care Campus	0	1	0	0	1
Phosphorus, Inc.	0	0	1	0	1
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine	0	0	1	0	1
Molecular Genetics, Sadra Medical Genetics Laboratory	1	0	0	0	1

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