Variants with conflicting interpretations "uncertain significance" from Michigan Medical Genetics Laboratories,University of Michigan and "likely benign" from Genome Diagnostics Laboratory,University Medical Center Utrecht

Minimum review status of the submission from Michigan Medical Genetics Laboratories,University of Michigan:		Collection method of the submission from Michigan Medical Genetics Laboratories,University of Michigan:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

Download table as spreadsheet

HGVS	dbSNP
NM_000059.3(BRCA2):c.476-9dup	rs276174849
NM_000059.3(BRCA2):c.67+4T>C	rs373546450
NM_000059.4(BRCA2):c.9501+3A>T	rs61757642

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.