Variants studied for catecholaminergic polymorphic ventricular tachycardia 5

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
9	12	64	14	16	114

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
TRDN	9	12	64	14	16	114

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	2	3	45	8	0	58
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	0	0	7	6	8	21
Revvity Omics, Revvity	1	6	2	0	0	9
Genome-Nilou Lab	0	0	0	0	8	8
OMIM	7	0	0	0	0	7
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	1	5	0	0	6
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	4	0	0	4
Baylor Genetics	0	0	2	0	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	1	1	0	0	2
Mendelics	0	0	0	0	1	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	1	0	0	0	0	1
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin	1	0	0	0	0	1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center	0	1	0	0	0	1
New York Genome Center	0	0	1	0	0	1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	0	1	0	0	1
KardioGenetik, Herz- und Diabeteszentrum NRW	0	0	1	0	0	1

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