rs8192719

Orientation

plus

Stabilized

plus

Make rs8192719(C;C)

Make rs8192719(C;T)

Make rs8192719(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

41012868

Gene

CYP2B6

is a	snp
is	mentioned by
dbSNP	rs8192719
dbSNP (classic)	rs8192719
ClinGen	rs8192719
ebi	rs8192719
HLI	rs8192719
Exac	rs8192719
Gnomad	rs8192719
Varsome	rs8192719
LitVar	rs8192719
Map	rs8192719
PheGenI	rs8192719
Biobank	rs8192719
1000 genomes	rs8192719
hgdp	rs8192719
ensembl	rs8192719
geneview	rs8192719
scholar	rs8192719
google	rs8192719
pharmgkb	rs8192719
gwascentral	rs8192719
openSNP	rs8192719
23andMe	rs8192719
SNPshot	rs8192719
SNPdbe	rs8192719
MSV3d	rs8192719
GWAS Ctlg	rs8192719

GMAF

0.2727

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 20639527 ] Haplotype structure of CYP2B6 and association with plasma efavirenz concentrations in a Chilean HIV cohort

[PMID 19239339 ] Associations between CYP2B6 polymorphisms and pharmacokinetics after a single dose of nevirapine or efavirenz in African americans.

[PMID 19652719 ] Univariate/multivariate genome-wide association scans using data from families and unrelated samples.

[PMID 19659438 ] CYP2B6 variants and plasma efavirenz concentrations during antiretroviral therapy in Port-au-Prince, Haiti.

[PMID 19702646 ] Tests of association for quantitative traits in nuclear families using principal components to correct for population stratification.

[PMID 19956578 ] Family-based bivariate association tests for quantitative traits.

[PMID 20017988 ] A comparative study of three methods for detecting association of quantitative traits in samples of related subjects.

[PMID 20017990 ] Family-based genome-wide association study for simulated data of Framingham Heart Study.

[PMID 20018031 ] The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study.

[PMID 21245293 ] Correlated genotypes in friendship networks.

[PMID 23249875] Contribution of CYP2B6 alleles in explaining extreme (S)-methadone plasma levels: a CYP2B6 gene resequencing study