rs899967
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs899967(C;C) |
| Make rs899967(C;G) |
| Make rs899967(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 63192088 |
| Gene | BCL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs899967 |
| dbSNP (classic) | rs899967 |
| ClinGen | rs899967 |
| ebi | rs899967 |
| HLI | rs899967 |
| Exac | rs899967 |
| Gnomad | rs899967 |
| Varsome | rs899967 |
| LitVar | rs899967 |
| Map | rs899967 |
| PheGenI | rs899967 |
| Biobank | rs899967 |
| 1000 genomes | rs899967 |
| hgdp | rs899967 |
| ensembl | rs899967 |
| geneview | rs899967 |
| scholar | rs899967 |
| rs899967 | |
| pharmgkb | rs899967 |
| gwascentral | rs899967 |
| openSNP | rs899967 |
| 23andMe | rs899967 |
| SNPshot | rs899967 |
| SNPdbe | rs899967 |
| MSV3d | rs899967 |
| GWAS Ctlg | rs899967 |
| GMAF | 0.399 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 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 | C |
| P-val | 7E-6 |
| Odds Ratio | .04 [0.02-0.05] ug/L decrease |
