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rs1806649

From SNPedia

Orientationplus
Stabilizedplus
Make rs1806649(C;C)
Make rs1806649(C;T)
Make rs1806649(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position177253424
GeneNFE2L2
is asnp
is mentioned by
dbSNPrs1806649
ebirs1806649
HLIrs1806649
Exacrs1806649
Varsomers1806649
Maprs1806649
PheGenIrs1806649
hapmaprs1806649
1000 genomesrs1806649
hgdprs1806649
ensemblrs1806649
gopubmedrs1806649
geneviewrs1806649
scholarrs1806649
googlers1806649
pharmgkbrs1806649
gwascentralrs1806649
openSNPrs1806649
23andMers1806649
23andMe allrs1806649
SNP Nexus

SNPshotrs1806649
SNPdbers1806649
MSV3drs1806649
GWAS Ctlgrs1806649
GMAF0.1382
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22531667] PM10-induced hospital admissions for asthma and chronic obstructive pulmonary disease: the modifying effect of individual characteristics


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


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


[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.