List of variants reported as uncertain significance for Congenital prothrombin deficiency by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000506.5(F2):c.1814_1815del (p.His605fs)	rs776618390	0.00001
NM_000506.5(F2):c.1131-5C>T	rs1255363601
NM_000506.5(F2):c.1598G>A (p.Arg533Gln)	rs1361766713
NM_000506.5(F2):c.607A>G (p.Ser203Gly)	rs2064868698
NM_000506.5(F2):c.954T>G (p.Ser318Arg)	rs2134532792

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.