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rs2070959

From SNPedia

Orientationplus
Stabilizedplus
Make rs2070959(A;A)
Make rs2070959(A;G)
Make rs2070959(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position233693545
GeneUGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs2070959
ebirs2070959
HLIrs2070959
Exacrs2070959
Varsomers2070959
Maprs2070959
PheGenIrs2070959
hapmaprs2070959
1000 genomesrs2070959
hgdprs2070959
ensemblrs2070959
gopubmedrs2070959
geneviewrs2070959
scholarrs2070959
googlers2070959
pharmgkbrs2070959
gwascentralrs2070959
openSNPrs2070959
23andMers2070959
23andMe allrs2070959
SNP Nexus

SNPshotrs2070959
SNPdbers2070959
MSV3drs2070959
GWAS Ctlgrs2070959
GMAF0.2668
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20214591] Pharmacogenomics in aspirin intolerance


[PMID 18349273] UGT1A1 genetic polymorphisms, endogenous estrogen exposure, soy food intake, and endometrial cancer risk.


[PMID 18992148OA-icon.png] Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.


[PMID 18992263OA-icon.png] Colon tumor mutations and epigenetic changes associated with genetic polymorphism: insight into disease pathways.


[PMID 19223558OA-icon.png] Polymorphic variation in NFKB1 and other aspirin-related genes and risk of Hodgkin lymphoma.


[PMID 19437564OA-icon.png] No association between cyclooxygenase-2 and uridine diphosphate glucuronosyltransferase 1A6 genetic polymorphisms and colon cancer risk.


[PMID 20463881OA-icon.png] Digital quantification of human eye color highlights genetic association of three new loci.