rs16856785
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs16856785(C;C) |
| Make rs16856785(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 162130497 |
| Gene | LOC105371475, NOS1AP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16856785 |
| dbSNP (classic) | rs16856785 |
| ClinGen | rs16856785 |
| ebi | rs16856785 |
| HLI | rs16856785 |
| Exac | rs16856785 |
| Gnomad | rs16856785 |
| Varsome | rs16856785 |
| LitVar | rs16856785 |
| Map | rs16856785 |
| PheGenI | rs16856785 |
| Biobank | rs16856785 |
| 1000 genomes | rs16856785 |
| hgdp | rs16856785 |
| ensembl | rs16856785 |
| geneview | rs16856785 |
| scholar | rs16856785 |
| rs16856785 | |
| pharmgkb | rs16856785 |
| gwascentral | rs16856785 |
| openSNP | rs16856785 |
| 23andMe | rs16856785 |
| SNPshot | rs16856785 |
| SNPdbe | rs16856785 |
| MSV3d | rs16856785 |
| GWAS Ctlg | rs16856785 |
| GMAF | 0.2603 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19180230
] rs16847548 and rs16856785 strongly associated with QT interval
[PMID 19204306] Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.
