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rs59421388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs59421388(C;T)
Make rs59421388(T;T)
ReferenceGRCh37 37.1/131
Chromosome22
Position42523610
GeneCYP2D6
is asnp
is mentioned by
dbSNPrs59421388
ebirs59421388
HLIrs59421388
Exacrs59421388
Varsomers59421388
Maprs59421388
PheGenIrs59421388
hapmaprs59421388
1000 genomesrs59421388
hgdprs59421388
ensemblrs59421388
gopubmedrs59421388
geneviewrs59421388
scholarrs59421388
googlers59421388
pharmgkbrs59421388
gwascentralrs59421388
openSNPrs59421388
23andMers59421388
23andMe allrs59421388
SNP Nexus

SNPshotrs59421388
SNPdbers59421388
MSV3drs59421388
GWAS Ctlgrs59421388
GMAF0.02893
Max Magnitude0


GET Evidence
CYP2D6-V287M
aa_change Val287Met
aa_change_short V287M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary



[PMID 23133420OA-icon.png] Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.