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rs34097093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common on affy axiom data
Make rs34097093(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position41012465
GeneCYP2B6
is asnp
is mentioned by
dbSNPrs34097093
ebirs34097093
HLIrs34097093
Exacrs34097093
Varsomers34097093
Maprs34097093
PheGenIrs34097093
hapmaprs34097093
1000 genomesrs34097093
hgdprs34097093
ensemblrs34097093
gopubmedrs34097093
geneviewrs34097093
scholarrs34097093
googlers34097093
pharmgkbrs34097093
gwascentralrs34097093
openSNPrs34097093
23andMers34097093
23andMe allrs34097093
SNP Nexus

SNPshotrs34097093
SNPdbers34097093
MSV3drs34097093
GWAS Ctlgrs34097093
Max Magnitude0

Suspect: Variation suspected to be false positive due to artifacts of the presence of a paralogous sequence in the genome (Musumeci et al. 2010) (Sudmant et al. 2010) or evidence suggested sequencing error or computation artifacts.


ClinVar
Risk rs34097093(T;T)
Alt rs34097093(T;T)
Reference rs34097093(C;C)
Significance Drug-response
Disease Efavirenz response
Variation info
Gene CYP2B6
CLNDBN Efavirenz response
Reversed 0
HGVS NC_000019.9:g.41518370C>T
CLNSRC ClinVar IMU414
CLNACC RCV000133446.1,