rs11886999
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11886999(C;C) |
| Make rs11886999(C;T) |
| Make rs11886999(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 96176055 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11886999 |
| dbSNP (classic) | rs11886999 |
| ClinGen | rs11886999 |
| ebi | rs11886999 |
| HLI | rs11886999 |
| Exac | rs11886999 |
| Gnomad | rs11886999 |
| Varsome | rs11886999 |
| LitVar | rs11886999 |
| Map | rs11886999 |
| PheGenI | rs11886999 |
| Biobank | rs11886999 |
| 1000 genomes | rs11886999 |
| hgdp | rs11886999 |
| ensembl | rs11886999 |
| geneview | rs11886999 |
| scholar | rs11886999 |
| rs11886999 | |
| pharmgkb | rs11886999 |
| gwascentral | rs11886999 |
| openSNP | rs11886999 |
| 23andMe | rs11886999 |
| SNPshot | rs11886999 |
| SNPdbe | rs11886999 |
| MSV3d | rs11886999 |
| GWAS Ctlg | rs11886999 |
| GMAF | 0.2438 |
| 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 | 8E-6 |
| Odds Ratio | .04 [0.02-0.06] ug/L increase |
