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
22 2 1 0 2 27

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
SDHD 22 2 1 2 27

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance benign total
OMIM 19 0 0 0 19
Center for Human Genetics, Inc,Center for Human Genetics, Inc 3 1 0 0 4
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics,Children's Hospital of Philadelphia 0 0 1 2 3
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
Division of Medical Genetics, University of Washington 1 0 0 0 1

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