ClinVar Miner

List of variants reported as likely pathogenic for breast carcinoma by Leiden Open Variation Database

Included ClinVar conditions (60):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.2559C>T (p.Gly853=) rs180177115 0.00001
NM_024675.4(PALB2):c.2835-1G>C rs515726099
NM_024675.4(PALB2):c.3202-1G>C rs515726111
NM_024675.4(PALB2):c.48+1G>C rs515726118
NM_024675.4(PALB2):c.49-2A>T rs786203245
NM_024675.4(PALB2):c.93dup (p.Leu32fs) rs864622498
PALB2:c.2515-1G>T rs587776417

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.