rs2074238
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common on affy axiom data |
| Make rs2074238(C;T) |
| Make rs2074238(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2463573 |
| Gene | KCNQ1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2074238 |
| dbSNP (classic) | rs2074238 |
| ClinGen | rs2074238 |
| ebi | rs2074238 |
| HLI | rs2074238 |
| Exac | rs2074238 |
| Gnomad | rs2074238 |
| Varsome | rs2074238 |
| LitVar | rs2074238 |
| Map | rs2074238 |
| PheGenI | rs2074238 |
| Biobank | rs2074238 |
| 1000 genomes | rs2074238 |
| hgdp | rs2074238 |
| ensembl | rs2074238 |
| geneview | rs2074238 |
| scholar | rs2074238 |
| rs2074238 | |
| pharmgkb | rs2074238 |
| gwascentral | rs2074238 |
| openSNP | rs2074238 |
| 23andMe | rs2074238 |
| SNPshot | rs2074238 |
| SNPdbe | rs2074238 |
| MSV3d | rs2074238 |
| GWAS Ctlg | rs2074238 |
| GMAF | 0.04178 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | T |
| P-val | 3E-17 |
| Odds Ratio | 7.88 [6.16-9.59] msec decrease |
[PMID 23856471] Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.
