Rs6759892

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Orientationplus
Make rs6759892(G;G)
Make rs6759892(G;T)
Make rs6759892(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233693023
GeneUGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs6759892
Exacrs6759892
PheGenIrs6759892
nextbiors6759892
hapmaprs6759892
1000 genomesrs6759892
hgdprs6759892
ensemblrs6759892
gopubmedrs6759892
geneviewrs6759892
scholarrs6759892
googlers6759892
pharmgkbrs6759892
gwascentralrs6759892
openSNPrs6759892
23andMers6759892
23andMe allrs6759892
SNP Nexus

SNPshotrs6759892
SNPdbers6759892
MSV3drs6759892
GMAF0.3444
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 20214591] Pharmacogenomics in aspirin intolerance


[PMID 17424838] [Genetic polymorphisms of MPO, NQO1, GSTP1, UGT1A6 associated with susceptibility of chronic benzene poisoning].


[PMID 19267064] [Relationship between genetic polymorphisms of phase I and phase II metabolizing enzymes and DNA damage of workers exposed to vinyl chloride monomer].


GET Evidence
UGT1A6-S7A
aa_change Ser7Ala
aa_change_short S7A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary