ClinVar Miner

Variants studied for Paragangliomas 2

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 not provided total
4 10 31 4 1 2 50

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 not provided total
SDHAF2 4 10 31 4 1 2 50

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Baylor Genetics 1 6 25 0 0 0 32
Color Diagnostics, LLC DBA Color Health 3 2 0 2 0 0 7
Fulgent Genetics, Fulgent Genetics 0 0 3 2 0 0 5
GeneReviews 0 0 0 0 0 2 2
Institute of Human Genetics, University of Leipzig Medical Center 0 1 1 0 0 0 2
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 0 0 2 0 0 0 2
OMIM 1 0 0 0 0 0 1
Revvity Omics, Revvity Omics 0 1 0 0 0 0 1
Genome-Nilou Lab 0 0 0 0 1 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 1 0 0 0 1

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