rs2001350
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs2001350(A;G) |
| Make rs2001350(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 177235697 |
| Gene | NFE2L2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2001350 |
| dbSNP (classic) | rs2001350 |
| ClinGen | rs2001350 |
| ebi | rs2001350 |
| HLI | rs2001350 |
| Exac | rs2001350 |
| Gnomad | rs2001350 |
| Varsome | rs2001350 |
| LitVar | rs2001350 |
| Map | rs2001350 |
| PheGenI | rs2001350 |
| Biobank | rs2001350 |
| 1000 genomes | rs2001350 |
| hgdp | rs2001350 |
| ensembl | rs2001350 |
| geneview | rs2001350 |
| scholar | rs2001350 |
| rs2001350 | |
| pharmgkb | rs2001350 |
| gwascentral | rs2001350 |
| openSNP | rs2001350 |
| 23andMe | rs2001350 |
| SNPshot | rs2001350 |
| SNPdbe | rs2001350 |
| MSV3d | rs2001350 |
| GWAS Ctlg | rs2001350 |
| GMAF | 0.1451 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21774808
] An interaction between Nrf2 polymorphisms and smoking status affects annual decline in FEV1: a longitudinal retrospective cohort study
[PMID 20196834] Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease.
