rs1483757
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1483757(A;A) |
| Make rs1483757(A;G) |
| Make rs1483757(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 117323735 |
| Gene | NOS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1483757 |
| dbSNP (classic) | rs1483757 |
| ClinGen | rs1483757 |
| ebi | rs1483757 |
| HLI | rs1483757 |
| Exac | rs1483757 |
| Gnomad | rs1483757 |
| Varsome | rs1483757 |
| LitVar | rs1483757 |
| Map | rs1483757 |
| PheGenI | rs1483757 |
| Biobank | rs1483757 |
| 1000 genomes | rs1483757 |
| hgdp | rs1483757 |
| ensembl | rs1483757 |
| geneview | rs1483757 |
| scholar | rs1483757 |
| rs1483757 | |
| pharmgkb | rs1483757 |
| gwascentral | rs1483757 |
| openSNP | rs1483757 |
| 23andMe | rs1483757 |
| SNPshot | rs1483757 |
| SNPdbe | rs1483757 |
| MSV3d | rs1483757 |
| GWAS Ctlg | rs1483757 |
| GMAF | 0.45 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 21679499] Polymorphisms in the nitric oxide synthase 1 gene are associated with severe chronic rhinosinusitis
[PMID 18663495
] Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.
[PMID 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
[PMID 22153699] Variants within the nitric oxide synthase 1 gene are associated with stroke susceptibility.
[PMID 24082858] Association of nNOS Gene Polymorphism with Ischemic Stroke in Han Chinese of North China
