rs1160297
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1160297(C;C) |
| Make rs1160297(C;G) |
| Make rs1160297(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 53010182 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1160297 |
| dbSNP (classic) | rs1160297 |
| ClinGen | rs1160297 |
| ebi | rs1160297 |
| HLI | rs1160297 |
| Exac | rs1160297 |
| Gnomad | rs1160297 |
| Varsome | rs1160297 |
| LitVar | rs1160297 |
| Map | rs1160297 |
| PheGenI | rs1160297 |
| Biobank | rs1160297 |
| 1000 genomes | rs1160297 |
| hgdp | rs1160297 |
| ensembl | rs1160297 |
| geneview | rs1160297 |
| scholar | rs1160297 |
| rs1160297 | |
| pharmgkb | rs1160297 |
| gwascentral | rs1160297 |
| openSNP | rs1160297 |
| 23andMe | rs1160297 |
| SNPshot | rs1160297 |
| SNPdbe | rs1160297 |
| MSV3d | rs1160297 |
| GWAS Ctlg | rs1160297 |
| GMAF | 0.3425 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 17903294 ]
|
| Trait | Hemostatic factors and hematological phenotypes |
| Title | Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study |
| Risk Allele | |
| P-val | 9.9999999999999995E-7 |
| Odds Ratio | NR NR |
