Variants in gene VIPR2 - ClinVar Miner

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	not provided	total
0	0	36	6	5	1	47

Condition and significance breakdown #

Total conditions: 5

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Condition	uncertain significance	likely benign	benign	not provided	total
not specified	32	2	0	0	34
not provided	2	4	4	0	9
See cases	1	0	1	0	2
Myoepithelial tumor	1	0	0	0	1
Normal pregnancy	0	0	0	1	1

Submitter and significance breakdown #

Total submitters: 9

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Submitter	uncertain significance	likely benign	benign	not provided	total
Ambry Genetics	32	2	0	0	34
Labcorp Genetics (formerly Invitae), Labcorp	0	1	4	0	5
CeGaT Center for Human Genetics Tuebingen	0	3	0	0	3
Bionano Laboratories	2	0	0	0	2
Breakthrough Genomics, Breakthrough Genomics	0	0	2	0	2
ISCA site 1	1	0	0	0	1
ISCA Site 6	0	0	1	0	1
Institute of Molecular and Cell Biology, University of Tartu	0	0	0	1	1
Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine	1	0	0	0	1

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