rs1806649

Orientation

plus

Stabilized

plus

Make rs1806649(C;C)

Make rs1806649(C;T)

Make rs1806649(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

177253424

Gene

NFE2L2

is a	snp
is	mentioned by
dbSNP	rs1806649
dbSNP (classic)	rs1806649
ClinGen	rs1806649
ebi	rs1806649
HLI	rs1806649
Exac	rs1806649
Gnomad	rs1806649
Varsome	rs1806649
LitVar	rs1806649
Map	rs1806649
PheGenI	rs1806649
Biobank	rs1806649
1000 genomes	rs1806649
hgdp	rs1806649
ensembl	rs1806649
geneview	rs1806649
scholar	rs1806649
google	rs1806649
pharmgkb	rs1806649
gwascentral	rs1806649
openSNP	rs1806649
23andMe	rs1806649
SNPshot	rs1806649
SNPdbe	rs1806649
MSV3d	rs1806649
GWAS Ctlg	rs1806649

GMAF

0.1382

Max Magnitude

0

?

(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 19671143 ] Level and course of FEV1 in relation to polymorphisms in NFE2L2 and KEAP1 in the general population.

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

[PMID 25496089 ] 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.