List of variants reported as uncertain significance for congenital factor V deficiency by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.2232G>C (p.Leu744Phe)	rs2101820303
NM_000130.5(F5):c.2234A>G (p.Asn745Ser)	rs2101820299
NM_000130.5(F5):c.2837G>T (p.Arg946Ile)	rs2101819634
NM_000130.5(F5):c.3995T>C (p.Leu1332Pro)	rs1241060030
NM_000130.5(F5):c.4297C>T (p.Leu1433Phe)	rs2101817787
NM_000130.5(F5):c.5022del (p.Leu1675fs)	rs2101811710
NM_000130.5(F5):c.5594T>G (p.Leu1865Arg)	rs1659497927
NM_000130.5(F5):c.6010T>C (p.Trp2004Arg)	rs2101806568

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.