rs1137933
| Orientation | minus |
| Stabilized | minus |
| Make rs1137933(C;C) |
| Make rs1137933(C;T) |
| Make rs1137933(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 27778906 |
| Gene | NOS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1137933 |
| dbSNP (classic) | rs1137933 |
| ClinGen | rs1137933 |
| ebi | rs1137933 |
| HLI | rs1137933 |
| Exac | rs1137933 |
| Gnomad | rs1137933 |
| Varsome | rs1137933 |
| LitVar | rs1137933 |
| Map | rs1137933 |
| PheGenI | rs1137933 |
| Biobank | rs1137933 |
| 1000 genomes | rs1137933 |
| hgdp | rs1137933 |
| ensembl | rs1137933 |
| geneview | rs1137933 |
| scholar | rs1137933 |
| rs1137933 | |
| pharmgkb | rs1137933 |
| gwascentral | rs1137933 |
| openSNP | rs1137933 |
| 23andMe | rs1137933 |
| SNPshot | rs1137933 |
| SNPdbe | rs1137933 |
| MSV3d | rs1137933 |
| GWAS Ctlg | rs1137933 |
| GMAF | 0.2039 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19635578] NO role of NOS2A susceptibility polymorphisms in rheumatoid arthritis
[PMID 15726497
] Gene-environment interaction effects on the development of immune responses in the 1st year of life.
[PMID 17601350] A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.
[PMID 17955236] Influence of the inducible nitric oxide synthase gene (NOS2A) on inflammatory bowel disease susceptibility.
[PMID 18663495] Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.
[PMID 19131662] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
[PMID 19218192] Genetic risk factors for portopulmonary hypertension in patients with advanced liver disease.
[PMID 19263529] Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.
[PMID 19309520] Nitric oxide synthase 2A (NOS2A) polymorphisms are not associated with invasive pneumococcal disease.
[PMID 19330901] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.
[PMID 19559392] A candidate gene association study of 77 polymorphisms in migraine.
[PMID 20031567] An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.
[PMID 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
[PMID 24746566] Genetic variants in inducible nitric oxide synthase gene are associated with the risk of radiation-induced lung injury in lung cancer patients receiving definitive thoracic radiation
[PMID 30581791] Nitric Oxide Synthase 2 Polymorphisms (rs2779248T/C and rs1137933C/T) and the Risk of Type 2 Diabetes in Zahedan, Southeastern Iran.
