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rs139801276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs139801276(C;C)
Make rs139801276(C;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position41004303
GeneCYP2B6
is asnp
is mentioned by
dbSNPrs139801276
ebirs139801276
HLIrs139801276
Exacrs139801276
Varsomers139801276
Maprs139801276
PheGenIrs139801276
hapmaprs139801276
1000 genomesrs139801276
hgdprs139801276
ensemblrs139801276
gopubmedrs139801276
geneviewrs139801276
scholarrs139801276
googlers139801276
pharmgkbrs139801276
gwascentralrs139801276
openSNPrs139801276
23andMers139801276
23andMe allrs139801276
SNP Nexus

SNPshotrs139801276
SNPdbers139801276
MSV3drs139801276
GWAS Ctlgrs139801276
Max Magnitude0
ClinVar
Risk rs139801276(C;C)
Alt rs139801276(C;C)
Reference rs139801276(T;T)
Significance Drug-response
Disease Efavirenz response
Variation info
Gene CYP2B6
CLNDBN Efavirenz response
Reversed 0
HGVS NC_000019.9:g.41510208T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000106296.2,