rs7089580
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 |
Make rs7089580(A;T) |
Make rs7089580(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 94945466 |
Gene | CYP2C9 |
is a | snp |
is | mentioned by |
dbSNP | rs7089580 |
dbSNP (classic) | rs7089580 |
ClinGen | rs7089580 |
ebi | rs7089580 |
HLI | rs7089580 |
Exac | rs7089580 |
Gnomad | rs7089580 |
Varsome | rs7089580 |
LitVar | rs7089580 |
Map | rs7089580 |
PheGenI | rs7089580 |
Biobank | rs7089580 |
1000 genomes | rs7089580 |
hgdp | rs7089580 |
ensembl | rs7089580 |
geneview | rs7089580 |
scholar | rs7089580 |
rs7089580 | |
pharmgkb | rs7089580 |
gwascentral | rs7089580 |
openSNP | rs7089580 |
23andMe | rs7089580 |
SNPshot | rs7089580 |
SNPdbe | rs7089580 |
MSV3d | rs7089580 |
GWAS Ctlg | rs7089580 |
GMAF | 0.1423 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 21270790] associations with higher warfarin dose, namely, VKORC1-8191 (rs61162043, P = 0.0041) and 18786 in CYP2C9 (rs7089580, P = 0.035) independent of the previous associations with these genes
[PMID 22158446] Association of the GGCX (CAA)16/17 repeat polymorphism with higher warfarin dose requirements in African Americans.