List of variants reported as likely pathogenic for Breast and/or ovarian cancer by Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.2596C>T (p.Arg866Cys)	rs41286300	0.00011
NM_007294.4(BRCA1):c.4986+6T>C	rs80358086	0.00001
NM_000059.4(BRCA2):c.3G>T (p.Met1Ile)	rs80358650
NM_000059.4(BRCA2):c.6938-2A>G	rs81002863
NM_000059.4(BRCA2):c.9925G>T (p.Glu3309Ter)	rs80359251
NM_007294.4(BRCA1):c.4675+1G>A	rs80358044
NM_007294.4(BRCA1):c.5521A>C (p.Ser1841Arg)	rs80357299

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.