rs10027628
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common genotype |
| Make rs10027628(C;C) |
| Make rs10027628(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 94722806 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10027628 |
| dbSNP (classic) | rs10027628 |
| ClinGen | rs10027628 |
| ebi | rs10027628 |
| HLI | rs10027628 |
| Exac | rs10027628 |
| Gnomad | rs10027628 |
| Varsome | rs10027628 |
| LitVar | rs10027628 |
| Map | rs10027628 |
| PheGenI | rs10027628 |
| Biobank | rs10027628 |
| 1000 genomes | rs10027628 |
| hgdp | rs10027628 |
| ensembl | rs10027628 |
| geneview | rs10027628 |
| scholar | rs10027628 |
| rs10027628 | |
| pharmgkb | rs10027628 |
| gwascentral | rs10027628 |
| openSNP | rs10027628 |
| 23andMe | rs10027628 |
| SNPshot | rs10027628 |
| SNPdbe | rs10027628 |
| MSV3d | rs10027628 |
| GWAS Ctlg | rs10027628 |
| GMAF | 0.06887 |
| 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 | C |
| P-val | 6E-6 |
| Odds Ratio | 1.81 [1.05-2.57] unit decrease |
