List of variants reported as likely benign for Familial cancer of breast by Institute of Human Genetics, University of Leipzig Medical Center

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.4068G>A (p.Leu1356=)	rs28897724	0.00295
NM_000059.4(BRCA2):c.68-7T>A	rs81002830	0.00277
NM_000051.4(ATM):c.162T>C (p.Tyr54=)	rs3218690	0.00200
NM_000059.4(BRCA2):c.1792A>G (p.Thr598Ala)	rs28897710	0.00182
NM_024675.4(PALB2):c.2816T>G (p.Leu939Trp)	rs45478192	0.00121
NM_000059.4(BRCA2):c.978C>A (p.Ser326Arg)	rs28897706	0.00082
NM_004360.5(CDH1):c.2439+10C>T	rs35236080	0.00057
NM_032043.2(BRIP1):c.2097+8A>C	rs730881642	0.00001
NM_000059.4(BRCA2):c.2779A>G (p.Met927Val)	rs786201837
NM_000465.4(BARD1):c.1075_1095del (p.Leu359_Pro365del)	rs28997575
NM_032043.3(BRIP1):c.3737C>T (p.Pro1246Leu)	rs876660074

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.