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rs2189784

From SNPedia

Orientationplus
Stabilizedplus
Make rs2189784(A;A)
Make rs2189784(A;G)
Make rs2189784(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position15848390
is asnp
is mentioned by
dbSNPrs2189784
ebirs2189784
HLIrs2189784
Exacrs2189784
Varsomers2189784
Maprs2189784
PheGenIrs2189784
hapmaprs2189784
1000 genomesrs2189784
hgdprs2189784
ensemblrs2189784
gopubmedrs2189784
geneviewrs2189784
scholarrs2189784
googlers2189784
pharmgkbrs2189784
gwascentralrs2189784
openSNPrs2189784
23andMers2189784
23andMe allrs2189784
SNP Nexus

SNPshotrs2189784
SNPdbers2189784
MSV3drs2189784
GWAS Ctlgrs2189784
GMAF0.3526
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19741565] Effects of CYP4F2 genetic polymorphisms and haplotypes on clinical outcomes in patients initiated on warfarin therapy


[PMID 20504253OA-icon.png] Combined CYP2C9, VKORC1 and CYP4F2 frequencies among racial and ethnic groups


[PMID 18535201OA-icon.png] A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.