ClinVar Miner

Variants studied for Hyperparathyroidism 2 with jaw tumors

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
8 2 77 12 24 121

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
CDC73 8 2 77 11 24 120
B3GALT2, CDC73 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 75 8 22 105
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 3 4 7
OMIM 6 0 0 0 0 6
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 0 0 3 0 0 3
MGZ Medical Genetics Center 1 1 0 0 0 2
CSER _CC_NCGL, University of Washington 0 0 0 2 0 2
Human Genetics Unit, University Of Colombo 0 1 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 1 0 0 0 0 1

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