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rs8192709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs8192709(C;T)
Make rs8192709(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position40991369
GeneCYP2B6
is asnp
is mentioned by
dbSNPrs8192709
ebirs8192709
HLIrs8192709
Exacrs8192709
Varsomers8192709
Maprs8192709
PheGenIrs8192709
hapmaprs8192709
1000 genomesrs8192709
hgdprs8192709
ensemblrs8192709
gopubmedrs8192709
geneviewrs8192709
scholarrs8192709
googlers8192709
pharmgkbrs8192709
gwascentralrs8192709
openSNPrs8192709
23andMers8192709
23andMe allrs8192709
SNP Nexus

SNPshotrs8192709
SNPdbers8192709
MSV3drs8192709
GWAS Ctlgrs8192709
GMAF0.05326
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 21886015] Cytochrome P450 CYP2B6 genotypes and haplotypes in a Colombian population: identification of novel variant CYP2B6 alleles


[PMID 19076156OA-icon.png] Polymorphisms of drug-metabolizing enzymes (GST, CYP2B6 and CYP3A) affect the pharmacokinetics of thiotepa and tepa.


GET Evidence
CYP2B6-R22C
aa_change Arg22Cys
aa_change_short R22C
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0475925
summary



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