rs1687390
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1687390(A;A) |
Make rs1687390(A;G) |
Make rs1687390(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 114327608 |
Gene | ORM1 |
is a | snp |
is | mentioned by |
dbSNP | rs1687390 |
dbSNP (classic) | rs1687390 |
ClinGen | rs1687390 |
ebi | rs1687390 |
HLI | rs1687390 |
Exac | rs1687390 |
Gnomad | rs1687390 |
Varsome | rs1687390 |
LitVar | rs1687390 |
Map | rs1687390 |
PheGenI | rs1687390 |
Biobank | rs1687390 |
1000 genomes | rs1687390 |
hgdp | rs1687390 |
ensembl | rs1687390 |
geneview | rs1687390 |
scholar | rs1687390 |
rs1687390 | |
pharmgkb | rs1687390 |
gwascentral | rs1687390 |
openSNP | rs1687390 |
23andMe | rs1687390 |
SNPshot | rs1687390 |
SNPdbe | rs1687390 |
MSV3d | rs1687390 |
GWAS Ctlg | rs1687390 |
GMAF | 0.101 |
Max Magnitude | 0 |
[PMID 17048007] Association of warfarin dose with genes involved in its action and metabolism.
[PMID 18574025] The largest prospective warfarin-treated cohort supports genetic forecasting.
[PMID 18680736] Genetic factors contribute to patient-specific warfarin dose for Han Chinese.