rs1060822
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1060822(C;C) |
| Make rs1060822(C;T) |
| Make rs1060822(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 27765605 |
| Gene | NOS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1060822 |
| dbSNP (classic) | rs1060822 |
| ClinGen | rs1060822 |
| ebi | rs1060822 |
| HLI | rs1060822 |
| Exac | rs1060822 |
| Gnomad | rs1060822 |
| Varsome | rs1060822 |
| LitVar | rs1060822 |
| Map | rs1060822 |
| PheGenI | rs1060822 |
| Biobank | rs1060822 |
| 1000 genomes | rs1060822 |
| hgdp | rs1060822 |
| ensembl | rs1060822 |
| geneview | rs1060822 |
| scholar | rs1060822 |
| rs1060822 | |
| pharmgkb | rs1060822 |
| gwascentral | rs1060822 |
| openSNP | rs1060822 |
| 23andMe | rs1060822 |
| SNPshot | rs1060822 |
| SNPdbe | rs1060822 |
| MSV3d | rs1060822 |
| GWAS Ctlg | rs1060822 |
| GMAF | 0.3085 |
| Max Magnitude | 0 |
[PMID 19624767] Influence of inducible nitric oxide synthase polymorphisms in Japanese patients with non-alcoholic fatty liver disease
[PMID 21481004] Association between recurrent aphthous stomatitis and inheritance of a single-nucleotide polymorphism of the NOS2 gene encoding inducible nitric oxide synthase.
