rs17666963
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17666963(C;C) |
| Make rs17666963(C;T) |
| Make rs17666963(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 123447985 |
| Gene | LOC105378531 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17666963 |
| dbSNP (classic) | rs17666963 |
| ClinGen | rs17666963 |
| ebi | rs17666963 |
| HLI | rs17666963 |
| Exac | rs17666963 |
| Gnomad | rs17666963 |
| Varsome | rs17666963 |
| LitVar | rs17666963 |
| Map | rs17666963 |
| PheGenI | rs17666963 |
| Biobank | rs17666963 |
| 1000 genomes | rs17666963 |
| hgdp | rs17666963 |
| ensembl | rs17666963 |
| geneview | rs17666963 |
| scholar | rs17666963 |
| rs17666963 | |
| pharmgkb | rs17666963 |
| gwascentral | rs17666963 |
| openSNP | rs17666963 |
| 23andMe | rs17666963 |
| SNPshot | rs17666963 |
| SNPdbe | rs17666963 |
| MSV3d | rs17666963 |
| GWAS Ctlg | rs17666963 |
| GMAF | 0.09137 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23247143 ]
|
| Trait | Cardiac Troponin-T levels |
| Title | Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European americans and blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. |
| Risk Allele | T |
| P-val | 9E-6 |
| Odds Ratio | 2.28 [1.58-3.28] |
