rs1878406
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1878406(C;C) |
| Make rs1878406(C;T) |
| Make rs1878406(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 147472512 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1878406 |
| dbSNP (classic) | rs1878406 |
| ClinGen | rs1878406 |
| ebi | rs1878406 |
| HLI | rs1878406 |
| Exac | rs1878406 |
| Gnomad | rs1878406 |
| Varsome | rs1878406 |
| LitVar | rs1878406 |
| Map | rs1878406 |
| PheGenI | rs1878406 |
| Biobank | rs1878406 |
| 1000 genomes | rs1878406 |
| hgdp | rs1878406 |
| ensembl | rs1878406 |
| geneview | rs1878406 |
| scholar | rs1878406 |
| rs1878406 | |
| pharmgkb | rs1878406 |
| gwascentral | rs1878406 |
| openSNP | rs1878406 |
| 23andMe | rs1878406 |
| SNPshot | rs1878406 |
| SNPdbe | rs1878406 |
| MSV3d | rs1878406 |
| GWAS Ctlg | rs1878406 |
| GMAF | 0.1823 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21909108 ]
|
| Trait | |
| Title | Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. |
| Risk Allele | T |
| P-val | 7E-12 |
| Odds Ratio | 0.1993 [0.14-0.26] unit increase |
| GWAS snp | |
|---|---|
| PMID | [PMID 24262325]
|
| Trait | Coronary artery disease |
| Title | Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. |
| Risk Allele | T |
| P-val | 1E-6 |
| Odds Ratio | 1.10 [1.06-1.14] |
[PMID 26520901] Impact of carotid atherosclerosis loci on cardiovascular events
