rs2069919
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2069919(A;A) |
Make rs2069919(A;G) |
Make rs2069919(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 127421977 |
Gene | PROC |
is a | snp |
is | mentioned by |
dbSNP | rs2069919 |
dbSNP (classic) | rs2069919 |
ClinGen | rs2069919 |
ebi | rs2069919 |
HLI | rs2069919 |
Exac | rs2069919 |
Gnomad | rs2069919 |
Varsome | rs2069919 |
LitVar | rs2069919 |
Map | rs2069919 |
PheGenI | rs2069919 |
Biobank | rs2069919 |
1000 genomes | rs2069919 |
hgdp | rs2069919 |
ensembl | rs2069919 |
geneview | rs2069919 |
scholar | rs2069919 |
rs2069919 | |
pharmgkb | rs2069919 |
gwascentral | rs2069919 |
openSNP | rs2069919 |
23andMe | rs2069919 |
SNPshot | rs2069919 |
SNPdbe | rs2069919 |
MSV3d | rs2069919 |
GWAS Ctlg | rs2069919 |
GMAF | 0.2158 |
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.