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rs6726395

From SNPedia

Orientationplus
Stabilizedplus
Make rs6726395(A;A)
Make rs6726395(A;G)
Make rs6726395(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position177238501
GeneNFE2L2
is asnp
is mentioned by
dbSNPrs6726395
ebirs6726395
HLIrs6726395
Exacrs6726395
Varsomers6726395
Maprs6726395
PheGenIrs6726395
hapmaprs6726395
1000 genomesrs6726395
hgdprs6726395
ensemblrs6726395
gopubmedrs6726395
geneviewrs6726395
scholarrs6726395
googlers6726395
pharmgkbrs6726395
gwascentralrs6726395
openSNPrs6726395
23andMers6726395
23andMe allrs6726395
SNP Nexus

SNPshotrs6726395
SNPdbers6726395
MSV3drs6726395
GWAS Ctlgrs6726395
GMAF0.4518
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21774808OA-icon.png] An interaction between Nrf2 polymorphisms and smoking status affects annual decline in FEV1: a longitudinal retrospective cohort study


[PMID 19671143OA-icon.png] Level and course of FEV1 in relation to polymorphisms in NFE2L2 and KEAP1 in the general population.


[PMID 20196834OA-icon.png] Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease.


[PMID 23276910] Association between polymorphism of the NQO1, NOS3 and NFE2L2 genes and AMD


[PMID 24528044] Association of NRF2 Polymorphism with Cholangiocarcinoma Prognosis in Thai Patients


[PMID 27374075] Genetic variants of nuclear factor erythroid-derived 2-like 2 associated with the complications in Han descents with type 2 diabetes mellitus of Northeast China.