Variants studied for Brugada syndrome 2

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	not provided	total
4	0	25	11	1	2	35

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	uncertain significance	likely benign	benign	not provided	total
GPD1L	4	25	11	1	2	35

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	uncertain significance	likely benign	benign	not provided	total
Fulgent Genetics, Fulgent Genetics	0	19	8	0	0	27
OMIM	4	0	0	0	0	4
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	0	0	2	1	0	3
GeneReviews	0	0	0	0	2	2
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	2	0	0	0	2
Revvity Omics, Revvity	0	1	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	1	0	0	0	1
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	0	1	0	0	0	1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne	0	0	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	1	0	0	0	1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	1	0	0	0	1
SYNLAB MVZ HG Mannheim GmbH, Zentrum für Humangenetik Mannheim	0	1	0	0	0	1

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