ClinVar Miner

Variants studied for Paragangliomas 1

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
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
25 7 5 0 6 42

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
SDHD 21 6 5 5 36
LOC126861339, SDHD 4 1 0 1 6

Submitter and significance breakdown #

Total submitters: 16
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Submitter pathogenic likely pathogenic uncertain significance benign total
OMIM 19 0 0 0 19
Color Diagnostics, LLC DBA Color Health 1 0 1 4 6
Myriad Genetics, Inc. 5 0 0 0 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
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

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