Variants from Research Lab, National Institute of Public Health

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	association	total
0	0	29	0	0	5	34

Gene and significance breakdown #

Total genes and gene combinations: 3

Download table as spreadsheet

Gene or gene combination	uncertain significance	association	total
PRC1	19	2	21
ABCC1	9	3	12
LOC126862223, PRC1	1	0	1

Condition and significance breakdown #

Total conditions: 2

Download table as spreadsheet

Condition	uncertain significance	association	total
Familial cancer of breast	29	3	32
Breast carcinoma	0	2	2

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.