rs6721961
| Orientation | plus |
| Stabilized | plus |
| Make rs6721961(G;G) |
| Make rs6721961(G;T) |
| Make rs6721961(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 177265309 |
| Gene | NFE2L2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6721961 |
| dbSNP (classic) | rs6721961 |
| ClinGen | rs6721961 |
| ebi | rs6721961 |
| HLI | rs6721961 |
| Exac | rs6721961 |
| Gnomad | rs6721961 |
| Varsome | rs6721961 |
| LitVar | rs6721961 |
| Map | rs6721961 |
| PheGenI | rs6721961 |
| Biobank | rs6721961 |
| 1000 genomes | rs6721961 |
| hgdp | rs6721961 |
| ensembl | rs6721961 |
| geneview | rs6721961 |
| scholar | rs6721961 |
| rs6721961 | |
| pharmgkb | rs6721961 |
| gwascentral | rs6721961 |
| openSNP | rs6721961 |
| 23andMe | rs6721961 |
| SNPshot | rs6721961 |
| SNPdbe | rs6721961 |
| MSV3d | rs6721961 |
| GWAS Ctlg | rs6721961 |
| GMAF | 0.1501 |
| Max Magnitude | 0 |
[PMID 21774808
] An interaction between Nrf2 polymorphisms and smoking status affects annual decline in FEV1: a longitudinal retrospective cohort study
[PMID 22207565] Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population
[PMID 22668754] Polymorphisms in the transcription factor NRF2 and forearm vasodilator responses in humans
[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 21107315] Effect of NFE2L2 genetic polymorphism on the association between oral estrogen therapy and the risk of venous thromboembolism in postmenopausal women.
[PMID 23572560] Regulatory Nexus of Synthesis and Degradation Deciphers Cellular Nrf2 Expression Levels
[PMID 23718983] Cigarette Smoking Is Associated with Human Semen Quality in Synergy with Functional NRF2 Polymorphisms
[PMID 23176750] Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease
[PMID 24499375] Association of Oxidative Stress Related Genes with Idiopathic Recurrent Miscarriage
[PMID 22964583] Genetic polymorphisms and protein expression of NRF2 and Sulfiredoxin predict survival outcomes in breast cancer.
[PMID 23251429] Inflammation and immune-related candidate gene associations with acute lung injury susceptibility and severity: a validation study.
[PMID 23650051] Role of Nrf2 in cancer photodynamic therapy: regulation of human ABC transporter ABCG2.
[PMID 23734777] Lack of strong effect modification by NFE2L2/CYP3A5/ABO of the risk of venous thrombosis associated with oral hormone therapy.
[PMID 24904228] Polymorphism of Nrf2, an Antioxidative Gene, is Associated with Blood Pressure and Cardiovascular Mortality in Hemodialysis Patients
[PMID 24919441] Polymorphisms of NRF2 and NRF2 target genes in urinary bladder cancer patients
[PMID 24040073] SNP (-617C>A) in ARE-like loci of the NRF2 gene: a new biomarker for prognosis of lung adenocarcinoma in Japanese non-smoking women
[PMID 26204833] Association between the NF-E2 Related Factor 2 Gene Polymorphism and Oxidative Stress, Anti-Oxidative Status, and Newly-Diagnosed Type 2 Diabetes Mellitus in a Chinese Population
[PMID 26238954] A Preliminary Study on Racial Differences in HMOX1, NFE2L2, and TGFβ1 Gene Polymorphisms and Radiation-Induced Late Normal Tissue Toxicity
[PMID 27222475] Genetic polymorphism of the Nrf2 promoter region is associated with vitiligo risk in Han Chinese populations.
