rs12567209
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs12567209(A;A) |
| Make rs12567209(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 162066689 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12567209 |
| dbSNP (classic) | rs12567209 |
| ClinGen | rs12567209 |
| ebi | rs12567209 |
| HLI | rs12567209 |
| Exac | rs12567209 |
| Gnomad | rs12567209 |
| Varsome | rs12567209 |
| LitVar | rs12567209 |
| Map | rs12567209 |
| PheGenI | rs12567209 |
| Biobank | rs12567209 |
| 1000 genomes | rs12567209 |
| hgdp | rs12567209 |
| ensembl | rs12567209 |
| geneview | rs12567209 |
| scholar | rs12567209 |
| rs12567209 | |
| pharmgkb | rs12567209 |
| gwascentral | rs12567209 |
| openSNP | rs12567209 |
| 23andMe | rs12567209 |
| SNPshot | rs12567209 |
| SNPdbe | rs12567209 |
| MSV3d | rs12567209 |
| GWAS Ctlg | rs12567209 |
| GMAF | 0.1107 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19204306
] rs10494366, rs4657139 and rs16847548 were significantly associated with adjusted QT interval in whites. relative hazard of SCD associated with each C allele at rs16847548 was 1.31. rs12567209 was also independently associated with SCD in whites (relative hazard 0.57, 95% confidence interval 0.39 to 0.83, P=0.003). No significant associations observed in blacks.
[PMID 19180230] Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.
[PMID 19643915] Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study.
