Variants in gene GRIN3B - 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	total
0	0	172	9	7	187

Condition and significance breakdown #

Total conditions: 3

Download table as spreadsheet

Condition	uncertain significance	likely benign	benign	total
not specified	169	5	0	174
not provided	1	4	7	12
Neurodevelopmental disorder	2	0	0	2

Submitter and significance breakdown #

Total submitters: 7

Download table as spreadsheet

Submitter	uncertain significance	likely benign	benign	total
Ambry Genetics	169	5	0	174
Breakthrough Genomics, Breakthrough Genomics	0	0	7	7
GeneDx	0	0	4	4
CeGaT Center for Human Genetics Tuebingen	0	4	0	4
Labcorp Genetics (formerly Invitae), Labcorp	0	0	3	3
Institute of Human Genetics, University of Leipzig Medical Center	2	0	0	2
Revvity Omics, Revvity	1	0	0	1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.