rs17708472

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs17708472(A;A)

Make rs17708472(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31094032

Gene

VKORC1

is a	snp
is	mentioned by
dbSNP	rs17708472
dbSNP (classic)	rs17708472
ClinGen	rs17708472
ebi	rs17708472
HLI	rs17708472
Exac	rs17708472
Gnomad	rs17708472
Varsome	rs17708472
LitVar	rs17708472
Map	rs17708472
PheGenI	rs17708472
Biobank	rs17708472
1000 genomes	rs17708472
hgdp	rs17708472
ensembl	rs17708472
geneview	rs17708472
scholar	rs17708472
google	rs17708472
pharmgkb	rs17708472
gwascentral	rs17708472
openSNP	rs17708472
23andMe	rs17708472
SNPshot	rs17708472
SNPdbe	rs17708472
MSV3d	rs17708472
GWAS Ctlg	rs17708472

GMAF

0.118

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 21127708 ] Genetic Variation of VKORC1 and CYP4F2 Genes Related to Warfarin Maintenance Dose in Patients with Myocardial Infarction

[PMID 22118051] Genetic variants in CYP (-1A2, -2C9, -2C19, -3A4 and -3A5), VKORC1 and ABCB1 genes in a black South African population: a window into diversity

[PMID 18252229 ] Warfarin pharmacogenetics: CYP2C9 and VKORC1 genotypes predict different sensitivity and resistance frequencies in the Ashkenazi and Sephardi Jewish populations.

[PMID 18855533 ] VKORC1 polymorphisms, haplotypes and haplotype groups on warfarin dose among African-Americans and European-Americans.

[PMID 19436136 ] Association of sequence variations in vitamin K epoxide reductase and gamma-glutamyl carboxylase genes with biochemical measures of vitamin K status.

[PMID 23662025 ] Genetic variation and haplotype structure of the gene Vitamin K epoxide reductase complex, subunit 1 in the Tamilian population

ClinVar
Risk	rs17708472(A;A)
Alt	rs17708472(A;A)
Reference	Rs17708472(G;G)
Significance	Drug-response
Disease	warfarin response - Dosage
Variation	info
Gene	VKORC1
CLNDBN	warfarin response - Dosage
Reversed	0
HGVS	NC_000016.9:g.31105353G>A
CLNSRC	PharmGKB Clinical Annotation
CLNACC	RCV000211198.1,