List of variants in gene PALB2 reported as likely benign by University of Washington Department of Laboratory Medicine, University of Washington

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:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.2514+136T>C	rs187008421	0.00187
NM_024675.4(PALB2):c.2996+17T>C	rs180177128	0.00060
NM_024675.4(PALB2):c.2749-18C>T	rs182194007	0.00055
NM_024675.4(PALB2):c.3114-522T>C	rs869312611	0.00021
NM_024675.4(PALB2):c.48+398A>G	rs548322552	0.00015
NM_024675.4(PALB2):c.3350+1313G>A	rs772944926	0.00014
NM_024675.4(PALB2):c.2515-39A>G	rs372998520	0.00011
NM_024675.4(PALB2):c.3114-42G>T	rs515726106	0.00004
NM_024675.4(PALB2):c.1684+1290C>T	rs869312612	0.00003

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.