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rs373489637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs373489637(G;G)
Make rs373489637(G;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position41006968
GeneCYP2B6
is asnp
is mentioned by
dbSNPrs373489637
ebirs373489637
HLIrs373489637
Exacrs373489637
Varsomers373489637
Maprs373489637
PheGenIrs373489637
hapmaprs373489637
1000 genomesrs373489637
hgdprs373489637
ensemblrs373489637
gopubmedrs373489637
geneviewrs373489637
scholarrs373489637
googlers373489637
pharmgkbrs373489637
gwascentralrs373489637
openSNPrs373489637
23andMers373489637
23andMe allrs373489637
SNP Nexus

SNPshotrs373489637
SNPdbers373489637
MSV3drs373489637
GWAS Ctlgrs373489637
Max Magnitude0
ClinVar
Risk rs373489637(G;G)
Alt rs373489637(G;G)
Reference rs373489637(T;T)
Significance Drug-response
Disease Efavirenz response
Variation info
Gene CYP2B6
CLNDBN Efavirenz response
Reversed 0
HGVS NC_000019.9:g.41512873T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000106297.2,