List of variants reported as benign by ClinGen FBN1 Variant Curation Expert Panel, ClinGen

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000138.5(FBN1):c.986T>C (p.Ile329Thr)	rs12324002	0.00737
NM_000138.5(FBN1):c.3509G>A (p.Arg1170His)	rs137854475	0.00168
NM_000138.5(FBN1):c.2956G>A (p.Ala986Thr)	rs112287730	0.00107
NM_000138.5(FBN1):c.3422C>T (p.Pro1141Leu)	rs2228241	0.00057
NM_000138.5(FBN1):c.8363C>T (p.Thr2788Met)	rs143007898	0.00031
NM_000138.5(FBN1):c.4640C>T (p.Thr1547Ile)	rs183306990	0.00027
NM_000138.5(FBN1):c.79G>A (p.Ala27Thr)	rs25397	0.00019

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.