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rs35652124

From SNPedia

Orientationplus
Stabilizedplus
Make rs35652124(C;C)
Make rs35652124(C;T)
Make rs35652124(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position177265345
GeneNFE2L2
is asnp
is mentioned by
dbSNPrs35652124
ebirs35652124
HLIrs35652124
Exacrs35652124
Varsomers35652124
Maprs35652124
PheGenIrs35652124
hapmaprs35652124
1000 genomesrs35652124
hgdprs35652124
ensemblrs35652124
gopubmedrs35652124
geneviewrs35652124
scholarrs35652124
googlers35652124
pharmgkbrs35652124
gwascentralrs35652124
openSNPrs35652124
23andMers35652124
23andMe allrs35652124
SNP Nexus

SNPshotrs35652124
SNPdbers35652124
MSV3drs35652124
GWAS Ctlgrs35652124
GMAF0.3522
Max Magnitude

[PMID 22668754OA-icon.png] Polymorphisms in the transcription factor NRF2 and forearm vasodilator responses in humans


[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 23176750] Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease


[PMID 24904228OA-icon.png] Polymorphism of Nrf2, an Antioxidative Gene, is Associated with Blood Pressure and Cardiovascular Mortality in Hemodialysis Patients


[PMID 25496089OA-icon.png] Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson¿s disease ¿ a multicenter study


[PMID 27222475] Genetic polymorphism of the Nrf2 promoter region is associated with vitiligo risk in Han Chinese populations.