rs8049607
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8049607(C;C) |
| Make rs8049607(C;T) |
| Make rs8049607(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 11597897 |
| Gene | LITAF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8049607 |
| dbSNP (classic) | rs8049607 |
| ClinGen | rs8049607 |
| ebi | rs8049607 |
| HLI | rs8049607 |
| Exac | rs8049607 |
| Gnomad | rs8049607 |
| Varsome | rs8049607 |
| LitVar | rs8049607 |
| Map | rs8049607 |
| PheGenI | rs8049607 |
| Biobank | rs8049607 |
| 1000 genomes | rs8049607 |
| hgdp | rs8049607 |
| ensembl | rs8049607 |
| geneview | rs8049607 |
| scholar | rs8049607 |
| rs8049607 | |
| pharmgkb | rs8049607 |
| gwascentral | rs8049607 |
| openSNP | rs8049607 |
| 23andMe | rs8049607 |
| SNPshot | rs8049607 |
| SNPdbe | rs8049607 |
| MSV3d | rs8049607 |
| GWAS Ctlg | rs8049607 |
| GMAF | 0.4977 |
| 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 | 5E-15 |
| Odds Ratio | |
| 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 | 6E-15 |
| Odds Ratio | 1.25 [0.81-1.69] ms increase |
| GWAS snp | |
|---|---|
| PMID | [PMID 23166209]
|
| Trait | QT interval |
| Title | Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans. |
| Risk Allele | C |
| P-val | 7E-7 |
| Odds Ratio | 1.63 [0.98-2.28] unit decrease |
