List of variants reported as likely benign for Thrombophilia due to protein S deficiency, autosomal dominant by Illumina Laboratory Services, Illumina

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_000313.4(PROS1):c.*197C>T	rs182088150	0.01026
NM_000313.4(PROS1):c.1032C>T (p.Ile344=)	rs78449232	0.00981
NM_000313.4(PROS1):c.-62T>G	rs556711298	0.00328
NM_000313.4(PROS1):c.*992T>G	rs538711279	0.00263
NM_000313.4(PROS1):c.*454G>A	rs539871594	0.00256
NM_000313.4(PROS1):c.698G>A (p.Arg233Lys)	rs41267007	0.00202
NM_000313.4(PROS1):c.*469A>C	rs147496684	0.00164
NM_000313.4(PROS1):c.*380A>T	rs138546241	0.00133
NM_000313.4(PROS1):c.1494T>C (p.Asn498=)	rs76877671	0.00033
NM_000313.4(PROS1):c.1446C>T (p.Gly482=)	rs535201753	0.00003
NM_000313.4(PROS1):c.119G>T (p.Arg40Leu)	rs7614835

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.