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rs17880887

From SNPedia

Orientationminus
Stabilizedminus
Make rs17880887(A;A)
Make rs17880887(A;C)
Make rs17880887(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position31099180
is asnp
is mentioned by
dbSNPrs17880887
ebirs17880887
HLIrs17880887
Exacrs17880887
Varsomers17880887
Maprs17880887
PheGenIrs17880887
hapmaprs17880887
1000 genomesrs17880887
hgdprs17880887
ensemblrs17880887
gopubmedrs17880887
geneviewrs17880887
scholarrs17880887
googlers17880887
pharmgkbrs17880887
gwascentralrs17880887
openSNPrs17880887
23andMers17880887
23andMe allrs17880887
SNP Nexus

SNPshotrs17880887
SNPdbers17880887
MSV3drs17880887
GWAS Ctlgrs17880887
GMAF0.1552
Max Magnitude

[PMID 24324947OA-icon.png] VKORC1 and CYP2C9 Genotype Variations in Relation to Warfarin Dosing in Korean Stroke Patients


[PMID 18305455OA-icon.png] Use of pharmacogenetic and clinical factors to predict the therapeutic dose of warfarin.


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


[PMID 19228618OA-icon.png] Estimation of the warfarin dose with clinical and pharmacogenetic data.