rs9658490
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs9658490(C;C) |
| Make rs9658490(C;G) |
| Make rs9658490(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 117232493 |
| Gene | NOS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9658490 |
| dbSNP (classic) | rs9658490 |
| ClinGen | rs9658490 |
| ebi | rs9658490 |
| HLI | rs9658490 |
| Exac | rs9658490 |
| Gnomad | rs9658490 |
| Varsome | rs9658490 |
| LitVar | rs9658490 |
| Map | rs9658490 |
| PheGenI | rs9658490 |
| Biobank | rs9658490 |
| 1000 genomes | rs9658490 |
| hgdp | rs9658490 |
| ensembl | rs9658490 |
| geneview | rs9658490 |
| scholar | rs9658490 |
| rs9658490 | |
| pharmgkb | rs9658490 |
| gwascentral | rs9658490 |
| openSNP | rs9658490 |
| 23andMe | rs9658490 |
| SNPshot | rs9658490 |
| SNPdbe | rs9658490 |
| MSV3d | rs9658490 |
| GWAS Ctlg | rs9658490 |
| GMAF | 0.1846 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24323870
] Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by Phenotype
