rs10183914
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10183914(C;C) |
| Make rs10183914(C;T) |
| Make rs10183914(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 177232938 |
| Gene | NFE2L2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10183914 |
| dbSNP (classic) | rs10183914 |
| ClinGen | rs10183914 |
| ebi | rs10183914 |
| HLI | rs10183914 |
| Exac | rs10183914 |
| Gnomad | rs10183914 |
| Varsome | rs10183914 |
| LitVar | rs10183914 |
| Map | rs10183914 |
| PheGenI | rs10183914 |
| Biobank | rs10183914 |
| 1000 genomes | rs10183914 |
| hgdp | rs10183914 |
| ensembl | rs10183914 |
| geneview | rs10183914 |
| scholar | rs10183914 |
| rs10183914 | |
| pharmgkb | rs10183914 |
| gwascentral | rs10183914 |
| openSNP | rs10183914 |
| 23andMe | rs10183914 |
| SNPshot | rs10183914 |
| SNPdbe | rs10183914 |
| MSV3d | rs10183914 |
| GWAS Ctlg | rs10183914 |
| GMAF | 0.2557 |
| 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.
