Variants studied for Paragangliomas 1

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
31	8	5	0	7	50

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
SDHD	23	7	5	6	40
LOC126861339, SDHD	7	1	0	1	9
SDHA	1	0	0	0	1

Submitter and significance breakdown #

Total submitters: 21

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
OMIM	23	0	0	0	23
Myriad Genetics, Inc.	10	1	0	0	11
Color Diagnostics, LLC DBA Color Health	1	0	1	4	6
KCCC/NGS Laboratory, Kuwait Cancer Control Center	0	0	0	5	5
Center for Human Genetics, Inc, Center for Human Genetics, Inc	3	1	0	0	4
Genome-Nilou Lab	0	0	0	4	4
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia	0	0	1	2	3
MGZ Medical Genetics Center	1	1	1	0	3
St. Jude Molecular Pathology, St. Jude Children's Research Hospital	0	0	3	0	3
Genetics and Molecular Pathology, SA Pathology	2	0	0	0	2
3billion	0	2	0	0	2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	1	0	0	0	1
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine	1	0	0	0	1
UCLA Clinical Genomics Center, UCLA	1	0	0	0	1
Undiagnosed Diseases Network, NIH	1	0	0	0	1
Genetics, Medical University of Vienna	0	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	1	0	0	1
deCODE genetics, Amgen	0	1	0	0	1
Division of Medical Genetics, University of Washington	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	1	0	0	0	1
Department of Human Genetics, Hannover Medical School	1	0	0	0	1

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