rs10919035
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10919035(C;C) |
| Make rs10919035(C;T) |
| Make rs10919035(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 162274222 |
| Gene | NOS1AP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10919035 |
| dbSNP (classic) | rs10919035 |
| ClinGen | rs10919035 |
| ebi | rs10919035 |
| HLI | rs10919035 |
| Exac | rs10919035 |
| Gnomad | rs10919035 |
| Varsome | rs10919035 |
| LitVar | rs10919035 |
| Map | rs10919035 |
| PheGenI | rs10919035 |
| Biobank | rs10919035 |
| 1000 genomes | rs10919035 |
| hgdp | rs10919035 |
| ensembl | rs10919035 |
| geneview | rs10919035 |
| scholar | rs10919035 |
| rs10919035 | |
| pharmgkb | rs10919035 |
| gwascentral | rs10919035 |
| openSNP | rs10919035 |
| 23andMe | rs10919035 |
| SNPshot | rs10919035 |
| SNPdbe | rs10919035 |
| MSV3d | rs10919035 |
| GWAS Ctlg | rs10919035 |
| GMAF | 0.2603 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22682551
] Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia
[PMID 24922963] 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease
