rs11756438
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11756438(A;A) |
| Make rs11756438(A;C) |
| Make rs11756438(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 118672469 |
| Gene | CEP85L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11756438 |
| dbSNP (classic) | rs11756438 |
| ClinGen | rs11756438 |
| ebi | rs11756438 |
| HLI | rs11756438 |
| Exac | rs11756438 |
| Gnomad | rs11756438 |
| Varsome | rs11756438 |
| LitVar | rs11756438 |
| Map | rs11756438 |
| PheGenI | rs11756438 |
| Biobank | rs11756438 |
| 1000 genomes | rs11756438 |
| hgdp | rs11756438 |
| ensembl | rs11756438 |
| geneview | rs11756438 |
| scholar | rs11756438 |
| rs11756438 | |
| pharmgkb | rs11756438 |
| gwascentral | rs11756438 |
| openSNP | rs11756438 |
| 23andMe | rs11756438 |
| SNPshot | rs11756438 |
| SNPdbe | rs11756438 |
| MSV3d | rs11756438 |
| GWAS Ctlg | rs11756438 |
| GMAF | 0.3646 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
23andMe blog Influences QT interval
| GWAS snp | |
|---|---|
| PMID | [PMID 19305408 ]
|
| Trait | QT interval |
| Title | Common variants at ten loci influence QT interval duation in the QTGEN Study |
| Risk Allele | A |
| P-val | 5E-22 |
| Odds Ratio | 1.40 [1.06-1.74] msec increase |
