rs231906
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs231906(C;C) |
| Make rs231906(C;T) |
| Make rs231906(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2731379 |
| Gene | KCNQ1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs231906 |
| dbSNP (classic) | rs231906 |
| ClinGen | rs231906 |
| ebi | rs231906 |
| HLI | rs231906 |
| Exac | rs231906 |
| Gnomad | rs231906 |
| Varsome | rs231906 |
| LitVar | rs231906 |
| Map | rs231906 |
| PheGenI | rs231906 |
| Biobank | rs231906 |
| 1000 genomes | rs231906 |
| hgdp | rs231906 |
| ensembl | rs231906 |
| geneview | rs231906 |
| scholar | rs231906 |
| rs231906 | |
| pharmgkb | rs231906 |
| gwascentral | rs231906 |
| openSNP | rs231906 |
| 23andMe | rs231906 |
| SNPshot | rs231906 |
| SNPdbe | rs231906 |
| MSV3d | rs231906 |
| GWAS Ctlg | rs231906 |
| GMAF | 0.4591 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23166209 ]
|
| Trait | QT interval |
| Title | Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans. |
| Risk Allele | A |
| P-val | 2E-6 |
| Odds Ratio | 1.51 [0.88-2.14] unit increase |
