List of variants in gene FGB reported as benign for coagulation protein disease

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: 21

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_005141.5(FGB):c.*619T>C	rs2227439	0.91129
NM_005141.5(FGB):c.*1550C>T	rs1044291	0.25394
NM_005141.5(FGB):c.*422A>C	rs2227421	0.24213
NM_005141.5(FGB):c.567C>T (p.Ser189=)	rs6056	0.15358
NM_005141.4(FGB):c.1433G>A (p.Arg478Lys)	rs4220	0.15295
NM_005141.5(FGB):c.*1369G>A	rs2227426	0.14032
NM_005141.5(FGB):c.*1617A>T	rs2059503	0.14026
NM_005141.5(FGB):c.*1517T>C	rs2059502	0.14019
NM_005141.5(FGB):c.*447T>C	rs2227423	0.13969
NM_005141.5(FGB):c.1125C>T (p.Tyr375=)	rs4681	0.13958
NM_005141.5(FGB):c.*443G>A	rs2227422	0.02316
NM_005141.5(FGB):c.843G>T (p.Val281=)	rs6058	0.02166
NM_005141.5(FGB):c.*1752G>T	rs116381809	0.01354
NM_005141.5(FGB):c.318T>C (p.Cys106=)	rs6055	0.01339
NM_005141.5(FGB):c.291C>T (p.His97=)	rs6060	0.01330
NM_005141.5(FGB):c.*1070G>C	rs2227425	0.00766
NM_005141.5(FGB):c.1239C>T (p.Asp413=)	rs148950857	0.00364
NM_005141.5(FGB):c.*373G>A	rs2227420
NM_005141.5(FGB):c.*834del	rs57313183
NM_005141.5(FGB):c.*918C>G	rs2227424
NM_005141.5(FGB):c.959-13_959-10del	rs140114081

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.