Variants with conflicting interpretations "likely pathogenic" from Center for Medical Genetics Ghent, University of Ghent and "uncertain significance" from any submitter

Minimum review status of the submission from Center for Medical Genetics Ghent, University of Ghent:		Collection method of the submission from Center for Medical Genetics Ghent, University of Ghent:
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: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000138.5(FBN1):c.3508C>T (p.Arg1170Cys)	rs1366894709
NM_000138.5(FBN1):c.6491G>A (p.Cys2164Tyr)	rs1555395189
NM_000256.3(MYBPC3):c.821+5G>A	rs397516077
NM_000335.5(SCN5A):c.844C>T (p.Arg282Cys)	rs199473082
Single allele

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.