Rs2069526

From SNPedia
Jump to: navigation, search

Orientationplus
Geno Mag Summary
(G;G) CYP1A2*1K_-739T>G homozygote
(G;T) carrier of one CYP1A2*1K_-739T>G allele
(T;T) 0 normal
ReferenceGRCh38 38.1/141
Chromosome15
Position74749000
GeneCYP1A2
is asnp
is mentioned by
dbSNPrs2069526
PheGenIrs2069526
nextbiors2069526
hapmaprs2069526
1000 genomesrs2069526
hgdprs2069526
ensemblrs2069526
gopubmedrs2069526
geneviewrs2069526
scholarrs2069526
googlers2069526
pharmgkbrs2069526
gwascentralrs2069526
openSNPrs2069526
23andMers2069526
23andMe allrs2069526
SNP Nexus

SNPshotrs2069526
SNPdbers2069526
MSV3drs2069526
GMAF0.06382
Max Magnitude0
? (G;G) (G;T) (T;T) 28
rs2069526 is a SNP in the CYP1A2 gene.

The rs2069526(T) allele defines the CYP1A2*1K_-739T>G variant.



GET Evidence
rs2069526
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0625
summary



[PMID 25081684] Four Polymorphisms in the Cytochrome P450 1A2 (CYP1A2) Gene and Lung Cancer Risk: a Meta-analysis