rs7188697
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7188697(A;A) |
| Make rs7188697(A;G) |
| Make rs7188697(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 58588274 |
| Gene | CNOT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7188697 |
| dbSNP (classic) | rs7188697 |
| ClinGen | rs7188697 |
| ebi | rs7188697 |
| HLI | rs7188697 |
| Exac | rs7188697 |
| Gnomad | rs7188697 |
| Varsome | rs7188697 |
| LitVar | rs7188697 |
| Map | rs7188697 |
| PheGenI | rs7188697 |
| Biobank | rs7188697 |
| 1000 genomes | rs7188697 |
| hgdp | rs7188697 |
| ensembl | rs7188697 |
| geneview | rs7188697 |
| scholar | rs7188697 |
| rs7188697 | |
| pharmgkb | rs7188697 |
| gwascentral | rs7188697 |
| openSNP | rs7188697 |
| 23andMe | rs7188697 |
| SNPshot | rs7188697 |
| SNPdbe | rs7188697 |
| MSV3d | rs7188697 |
| GWAS Ctlg | rs7188697 |
| GMAF | 0.2897 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | A |
| P-val | 7E-25 |
| Odds Ratio | 1.66 [1.20-2.12] ms increase |
