rs4657178
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4657178(C;C) |
| Make rs4657178(C;T) |
| Make rs4657178(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 162240820 |
| Gene | NOS1AP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4657178 |
| dbSNP (classic) | rs4657178 |
| ClinGen | rs4657178 |
| ebi | rs4657178 |
| HLI | rs4657178 |
| Exac | rs4657178 |
| Gnomad | rs4657178 |
| Varsome | rs4657178 |
| LitVar | rs4657178 |
| Map | rs4657178 |
| PheGenI | rs4657178 |
| Biobank | rs4657178 |
| 1000 genomes | rs4657178 |
| hgdp | rs4657178 |
| ensembl | rs4657178 |
| geneview | rs4657178 |
| scholar | rs4657178 |
| rs4657178 | |
| pharmgkb | rs4657178 |
| gwascentral | rs4657178 |
| openSNP | rs4657178 |
| 23andMe | rs4657178 |
| SNPshot | rs4657178 |
| SNPdbe | rs4657178 |
| MSV3d | rs4657178 |
| GWAS Ctlg | rs4657178 |
| GMAF | 0.3797 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19305409 ]
|
| Trait | QT interval |
| Title | Common variants at ten loci modulate the QT interval duration in the QTSCD Study |
| Risk Allele | T |
| P-val | 7E-33 |
| Odds Ratio | 2.19 [1.76-2.62] ms increase |
