rs1800779
| Orientation | plus |
| Stabilized | plus |
| Make rs1800779(A;A) |
| Make rs1800779(A;G) |
| Make rs1800779(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 150992855 |
| Gene | NOS3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800779 |
| dbSNP (classic) | rs1800779 |
| ClinGen | rs1800779 |
| ebi | rs1800779 |
| HLI | rs1800779 |
| Exac | rs1800779 |
| Gnomad | rs1800779 |
| Varsome | rs1800779 |
| LitVar | rs1800779 |
| Map | rs1800779 |
| PheGenI | rs1800779 |
| Biobank | rs1800779 |
| 1000 genomes | rs1800779 |
| hgdp | rs1800779 |
| ensembl | rs1800779 |
| geneview | rs1800779 |
| scholar | rs1800779 |
| rs1800779 | |
| pharmgkb | rs1800779 |
| gwascentral | rs1800779 |
| openSNP | rs1800779 |
| 23andMe | rs1800779 |
| SNPshot | rs1800779 |
| SNPdbe | rs1800779 |
| MSV3d | rs1800779 |
| GWAS Ctlg | rs1800779 |
| GMAF | 0.2502 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19815736
] The Relation between Endothelial Nitric Oxide Synthase Gene Variants and Primary Open-Angle Glaucoma: Interactions with Gender and Postmenopausal Hormone Use
[PMID 20409549] NOS3 gene polymorphisms are associated with risk markers of cardiovascular disease, and interact with omega-3 polyunsaturated fatty acids
[PMID 21122033] Leukoaraiosis is associated with genes regulating blood-brain barrier homeostasis in ischaemic stroke patients
[PMID 21291465] The association of genetic polymorphisms with cerebral palsy: a meta-analysis
[PMID 15726497] Gene-environment interaction effects on the development of immune responses in the 1st year of life.
[PMID 18069999] Renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms are not associated with the risk of incident type 2 diabetes mellitus: a prospective cohort study.
[PMID 18246059] Habitual energy expenditure modifies the association between NOS3 gene polymorphisms and blood pressure.
[PMID 18513389] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.
[PMID 18687083] Lack of association of endothelial nitric oxide synthase polymorphisms and migraine.
[PMID 18698212] Association of renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms with blood pressure progression and incident hypertension: prospective cohort study.
[PMID 19131662] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
[PMID 19263529] Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.
[PMID 19330901] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.
[PMID 19493349] 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.
[PMID 19559392] A candidate gene association study of 77 polymorphisms in migraine.
[PMID 19584173] Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA study.
[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 21674837] Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.
[PMID 24192154] Nitric oxide synthase polymorphisms, gene expression and lung function in chronic obstructive pulmonary disease
[PMID 23826716] Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis.
[PMID 25140814] Association of NOS3 gene variants and clinical contributors of hypoxic-ischemic encephalopathy
[PMID 28070505] The Association between NOS3 Gene Polymorphisms and Hypoxic-Ischemic Encephalopathy Susceptibility and Symptoms in Chinese Han Population.
