rs11970286
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11970286(C;C) |
| Make rs11970286(C;T) |
| Make rs11970286(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 118359211 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11970286 |
| dbSNP (classic) | rs11970286 |
| ClinGen | rs11970286 |
| ebi | rs11970286 |
| HLI | rs11970286 |
| Exac | rs11970286 |
| Gnomad | rs11970286 |
| Varsome | rs11970286 |
| LitVar | rs11970286 |
| Map | rs11970286 |
| PheGenI | rs11970286 |
| Biobank | rs11970286 |
| 1000 genomes | rs11970286 |
| hgdp | rs11970286 |
| ensembl | rs11970286 |
| geneview | rs11970286 |
| scholar | rs11970286 |
| rs11970286 | |
| pharmgkb | rs11970286 |
| gwascentral | rs11970286 |
| openSNP | rs11970286 |
| 23andMe | rs11970286 |
| SNPshot | rs11970286 |
| SNPdbe | rs11970286 |
| MSV3d | rs11970286 |
| GWAS Ctlg | rs11970286 |
| GMAF | 0.3095 |
| 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 | 2E-24 |
| Odds Ratio | 1.64 [1.25-2.03] ms increase |
| GWAS snp | |
|---|---|
| PMID | [PMID 20062063] |
| Trait | Electrocardiographic traits |
| Title | Several common variants modulate heart rate, PR interval and QRS duration |
| Risk Allele | T |
| P-val | 8E-7 |
| Odds Ratio | 6.19 [3.73-8.65] % SD increase |
