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rs373000587

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373000587(A;A)
Make rs373000587(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome22
GeneCYP2D6
is asnp
is mentioned by
dbSNPrs373000587
ebirs373000587
HLIrs373000587
Exacrs373000587
Varsomers373000587
Maprs373000587
PheGenIrs373000587
hapmaprs373000587
1000 genomesrs373000587
hgdprs373000587
ensemblrs373000587
gopubmedrs373000587
geneviewrs373000587
scholarrs373000587
googlers373000587
pharmgkbrs373000587
gwascentralrs373000587
openSNPrs373000587
23andMers373000587
23andMe allrs373000587
SNP Nexus

SNPshotrs373000587
SNPdbers373000587
MSV3drs373000587
GWAS Ctlgrs373000587
Max Magnitude0
ClinVar
Risk rs373000587(A,T;A,T)
Alt rs373000587(A,T;A,T)
Reference rs373000587(C;C)
Significance Drug-response
Disease not provided
Variation info
Gene CYP2D6
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.42525172C>A
CLNSRC
CLNACC RCV000162081.1,