List of variants reported as drug response for coumarin resistance

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: 22

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_000016.10:g.31096368=	rs9923231	0.68843
NC_000019.10:g.44911194T>C	rs439401	0.68512
NC_000019.10:g.44905579T>G	rs405509	0.58661
NM_000041.4(APOE):c.43+520G>A	rs769450	0.39475
NM_000384.3(APOB):c.7545C>T (p.Thr2515=)	rs693	0.38722
NM_024006.4(VKORC1):c.-1639G>A	rs9923231	0.31157
NM_024006.6(VKORC1):c.174-136C>T	rs9934438	0.31147
NM_000041.4(APOE):c.388T>C (p.Cys130Arg)	rs429358	0.16059
CYP2C9*2	rs1799853	0.08975
NM_000041.2(APOE):c.526C>T (p.Arg176Cys)	rs7412	0.07986
CYP2C9*3	rs1057910	0.04900
NM_000762.5(CYP2A6):c.479T>A (p.Leu160His)	rs1801272	0.01863
CYP2A6*12A
NG_011564.1(VKORC1):g.3639dup	rs397509427
NM_000384.3(APOB):c.13013G>A (p.Ser4338Asn)
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp)
NM_000384.3(APOB):c.1853C>T (p.Ala618Val)
NM_000384.3(APOB):c.293C>T (p.Thr98Ile)
NM_000771.3(CYP2C9):c.[430C=;1075A=]
NM_000771.3(CYP2C9):c.[430C=;1075A>C]
NM_000771.3(CYP2C9):c.[430C>T;1075A=]
NM_024006.6(VKORC1):c.383T>G (p.Leu128Arg)	rs104894542

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.