rs1800783
| Orientation | plus |
| Stabilized | plus |
| Make rs1800783(A;A) |
| Make rs1800783(A;T) |
| Make rs1800783(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 150992309 |
| Gene | NOS3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800783 |
| dbSNP (classic) | rs1800783 |
| ClinGen | rs1800783 |
| ebi | rs1800783 |
| HLI | rs1800783 |
| Exac | rs1800783 |
| Gnomad | rs1800783 |
| Varsome | rs1800783 |
| LitVar | rs1800783 |
| Map | rs1800783 |
| PheGenI | rs1800783 |
| Biobank | rs1800783 |
| 1000 genomes | rs1800783 |
| hgdp | rs1800783 |
| ensembl | rs1800783 |
| geneview | rs1800783 |
| scholar | rs1800783 |
| rs1800783 | |
| pharmgkb | rs1800783 |
| gwascentral | rs1800783 |
| openSNP | rs1800783 |
| 23andMe | rs1800783 |
| SNPshot | rs1800783 |
| SNPdbe | rs1800783 |
| MSV3d | rs1800783 |
| GWAS Ctlg | rs1800783 |
| GMAF | 0.332 |
| Max Magnitude | 0 |
Note: this SNP should perhaps be best seen as a proxy for rs4496877, a SNP assayed by the Illumina 1M chip. The pairwise r(2) linkage between the two is reported to be 0.96.[PMID 20962522]
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19853644] Promoter polymorphisms of the NOS3 gene are associated with hypnotizability-dependent vascular response to nociceptive stimulation
[PMID 20409549] NOS3 gene polymorphisms are associated with risk markers of cardiovascular disease, and interact with omega-3 polyunsaturated fatty acids
[PMID 20962522] Genetic Polymorphisms in Nitric Oxide Synthase 3 Gene and Implications for Kidney Disease: A Meta-Analysis
[PMID 17980690
] Polymorphisms in the endothelial nitric oxide synthase gene and bone density/ultrasound and geometry in humans.
[PMID 18246059] Habitual energy expenditure modifies the association between NOS3 gene polymorphisms and blood pressure.
[PMID 18663495] Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.
[PMID 21252862] NOS3 variants, physical activity, and blood pressure in the European Youth Heart Study.
[PMID 21674837] Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.
[PMID 23021696] Single-nucleotide polymorphisms in genes involved in placental function and unexplained stillbirth
[PMID 24035903] The -974 C>A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients
[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.
