rs2886161
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2886161(C;C) |
Make rs2886161(C;T) |
Make rs2886161(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 177263111 |
Gene | NFE2L2 |
is a | snp |
is | mentioned by |
dbSNP | rs2886161 |
dbSNP (classic) | rs2886161 |
ClinGen | rs2886161 |
ebi | rs2886161 |
HLI | rs2886161 |
Exac | rs2886161 |
Gnomad | rs2886161 |
Varsome | rs2886161 |
LitVar | rs2886161 |
Map | rs2886161 |
PheGenI | rs2886161 |
Biobank | rs2886161 |
1000 genomes | rs2886161 |
hgdp | rs2886161 |
ensembl | rs2886161 |
geneview | rs2886161 |
scholar | rs2886161 |
rs2886161 | |
pharmgkb | rs2886161 |
gwascentral | rs2886161 |
openSNP | rs2886161 |
23andMe | rs2886161 |
SNPshot | rs2886161 |
SNPdbe | rs2886161 |
MSV3d | rs2886161 |
GWAS Ctlg | rs2886161 |
GMAF | 0.3512 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24528044] Association of NRF2 Polymorphism with Cholangiocarcinoma Prognosis in Thai Patients
[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