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rs2070999

From SNPedia

Orientationplus
Stabilizedplus
Make rs2070999(A;A)
Make rs2070999(A;G)
Make rs2070999(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position2999495
GeneNQO2
is asnp
is mentioned by
dbSNPrs2070999
ebirs2070999
HLIrs2070999
Exacrs2070999
Varsomers2070999
Maprs2070999
PheGenIrs2070999
hapmaprs2070999
1000 genomesrs2070999
hgdprs2070999
ensemblrs2070999
gopubmedrs2070999
geneviewrs2070999
scholarrs2070999
googlers2070999
pharmgkbrs2070999
gwascentralrs2070999
openSNPrs2070999
23andMers2070999
23andMe allrs2070999
SNP Nexus

SNPshotrs2070999
SNPdbers2070999
MSV3drs2070999
GWAS Ctlgrs2070999
GMAF0.3007
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24354914] NQO1 rs1800566 C>T polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population


[PMID 23054000] Genetic variants in metabolizing genes NQO1, NQO2, MTHFR and risk of prostate cancer: a study from North India.