List of variants reported as uncertain significance for hemophilia A by Genetics and Molecular Pathology, SA Pathology

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.1018G>A (p.Glu340Lys)	rs781954986	0.00019
NM_000132.4(F8):c.1337G>A (p.Arg446Gln)	rs781889613	0.00010
NM_000132.4(F8):c.1573G>A (p.Gly525Arg)	rs1357976820	0.00001
NM_000132.4(F8):c.456C>G (p.Ser152Arg)	rs781912033	0.00001
NM_000132.4(F8):c.102C>G (p.Asp34Glu)
NM_000132.4(F8):c.1468A>G (p.Arg490Gly)	rs1603435026
NM_000132.4(F8):c.2150G>T (p.Arg717Leu)	rs942909873
NM_000132.4(F8):c.5146C>A (p.His1716Asn)	rs2073172888
NM_000132.4(F8):c.5582A>G (p.Asp1861Gly)	rs2123997685
NM_000132.4(F8):c.6362T>A (p.Ile2121Asn)
NM_000552.5(VWF):c.2308C>T (p.Pro770Ser)

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.