Variants studied for Hyperparathyroidism 2 with jaw tumors

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
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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