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rs4653436

From SNPedia

Orientationplus
Stabilizedplus
Make rs4653436(A;A)
Make rs4653436(A;G)
Make rs4653436(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position225807509
is asnp
is mentioned by
dbSNPrs4653436
ebirs4653436
HLIrs4653436
Exacrs4653436
Varsomers4653436
Maprs4653436
PheGenIrs4653436
hapmaprs4653436
1000 genomesrs4653436
hgdprs4653436
ensemblrs4653436
gopubmedrs4653436
geneviewrs4653436
scholarrs4653436
googlers4653436
pharmgkbrs4653436
gwascentralrs4653436
openSNPrs4653436
23andMers4653436
23andMe allrs4653436
SNP Nexus

SNPshotrs4653436
SNPdbers4653436
MSV3drs4653436
GWAS Ctlgrs4653436
GMAF0.2672
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20842355] VKORC1-1639G>A, CYP2C9, EPHX1691A>G genotype, body weight, and age are important predictors for warfarin maintenance doses in patients with mechanical heart valve prostheses in southwest China



[PMID 17048007OA-icon.png] Association of warfarin dose with genes involved in its action and metabolism.


[PMID 18574025OA-icon.png] The largest prospective warfarin-treated cohort supports genetic forecasting.


[PMID 18680736] Genetic factors contribute to patient-specific warfarin dose for Han Chinese.


GET Evidence
rs4653436
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.206349
summary