rs8068149
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8068149(A;A) |
| Make rs8068149(A;G) |
| Make rs8068149(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 27761829 |
| Gene | NOS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8068149 |
| dbSNP (classic) | rs8068149 |
| ClinGen | rs8068149 |
| ebi | rs8068149 |
| HLI | rs8068149 |
| Exac | rs8068149 |
| Gnomad | rs8068149 |
| Varsome | rs8068149 |
| LitVar | rs8068149 |
| Map | rs8068149 |
| PheGenI | rs8068149 |
| Biobank | rs8068149 |
| 1000 genomes | rs8068149 |
| hgdp | rs8068149 |
| ensembl | rs8068149 |
| geneview | rs8068149 |
| scholar | rs8068149 |
| rs8068149 | |
| pharmgkb | rs8068149 |
| gwascentral | rs8068149 |
| openSNP | rs8068149 |
| 23andMe | rs8068149 |
| SNPshot | rs8068149 |
| SNPdbe | rs8068149 |
| MSV3d | rs8068149 |
| GWAS Ctlg | rs8068149 |
| GMAF | 0.4596 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18563708] Family-based association study between NOS-I and -IIA polymorphisms and autism spectrum disorders in Korean trios.
[PMID 19309520
] Nitric oxide synthase 2A (NOS2A) polymorphisms are not associated with invasive pneumococcal disease.
