rs2682826
| Orientation | minus |
| Stabilized | minus |
| Make rs2682826(C;C) |
| Make rs2682826(C;T) |
| Make rs2682826(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 117215033 |
| Gene | NOS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2682826 |
| dbSNP (classic) | rs2682826 |
| ClinGen | rs2682826 |
| ebi | rs2682826 |
| HLI | rs2682826 |
| Exac | rs2682826 |
| Gnomad | rs2682826 |
| Varsome | rs2682826 |
| LitVar | rs2682826 |
| Map | rs2682826 |
| PheGenI | rs2682826 |
| Biobank | rs2682826 |
| 1000 genomes | rs2682826 |
| hgdp | rs2682826 |
| ensembl | rs2682826 |
| geneview | rs2682826 |
| scholar | rs2682826 |
| rs2682826 | |
| pharmgkb | rs2682826 |
| gwascentral | rs2682826 |
| openSNP | rs2682826 |
| 23andMe | rs2682826 |
| SNPshot | rs2682826 |
| SNPdbe | rs2682826 |
| MSV3d | rs2682826 |
| GWAS Ctlg | rs2682826 |
| GMAF | 0.258 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19513863] No association between polymorphisms of neuronal oxide synthase 1 gene (NOS1) and schizophrenia in a Japanese population
[PMID 20470850] A common polymorphism in the 3'-UTR of the NOS1 gene was associated with completed suicides in Japanese male population
[PMID 21641795] Genetic polymorphisms in DNA repair and oxidative stress pathways associated with malignant melanoma susceptibility
[PMID 17579350] NOS-I and -III gene variants are differentially associated with facets of suicidal behavior and aggression-related traits.
[PMID 18663495
] Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.
[PMID 21172166
] Pharmacogenetics of antidepressant response.
[PMID 21577011] NCAM1, TACR1 and NOS genes and temperament: a study on suicide attempters and controls.
[PMID 24114042] Nitric Oxide Synthase Gene Polymorphisms in Functional Dyspepsia
[PMID 24602444
] Analysis of nitric oxide synthase gene polymorphisms in neonatal respiratory distress syndrome among the Chinese Han population
[PMID 23826716] Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis.
