rs3918226
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs3918226(C;T) |
| Make rs3918226(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 150993088 |
| Gene | NOS3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3918226 |
| dbSNP (classic) | rs3918226 |
| ClinGen | rs3918226 |
| ebi | rs3918226 |
| HLI | rs3918226 |
| Exac | rs3918226 |
| Gnomad | rs3918226 |
| Varsome | rs3918226 |
| LitVar | rs3918226 |
| Map | rs3918226 |
| PheGenI | rs3918226 |
| Biobank | rs3918226 |
| 1000 genomes | rs3918226 |
| hgdp | rs3918226 |
| ensembl | rs3918226 |
| geneview | rs3918226 |
| scholar | rs3918226 |
| rs3918226 | |
| pharmgkb | rs3918226 |
| gwascentral | rs3918226 |
| openSNP | rs3918226 |
| 23andMe | rs3918226 |
| SNPshot | rs3918226 |
| SNPdbe | rs3918226 |
| MSV3d | rs3918226 |
| GWAS Ctlg | rs3918226 |
| GMAF | 0.04316 |
| Max Magnitude | 0 |
[PMID 19559392
] A candidate gene association study of 77 polymorphisms in migraine
[PMID 21291465] The association of genetic polymorphisms with cerebral palsy: a meta-analysis
[PMID 17367796] Association of polymorphisms in NOS3 with the ankle-brachial index in hypertensive adults.
[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 18513389] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.
[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 19619703] Association of genetic variants with the metabolic syndrome in 20,806 white women: The Women's Health Genome 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 21332392] Endothelial nitric oxide synthase haplotypes associated with aura in patients with migraine.
[PMID 22184326] Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.
[PMID 22388798] Gene panels to help identify subgroups at high and low risk of coronary heart disease among those randomized to antihypertensive treatment: the GenHAT study.
[PMID 22547447] Endothelial nitric oxide synthase polymorphism rs3918226 associated with hypertension does not affect plasma nitrite levels in healthy subjects.
[PMID 22865486] Interaction among nitric oxide (NO)-related genes in migraine susceptibility.
