rs7159841
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7159841(C;C) |
| Make rs7159841(C;T) |
| Make rs7159841(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 47394632 |
| Gene | MDGA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7159841 |
| dbSNP (classic) | rs7159841 |
| ClinGen | rs7159841 |
| ebi | rs7159841 |
| HLI | rs7159841 |
| Exac | rs7159841 |
| Gnomad | rs7159841 |
| Varsome | rs7159841 |
| LitVar | rs7159841 |
| Map | rs7159841 |
| PheGenI | rs7159841 |
| Biobank | rs7159841 |
| 1000 genomes | rs7159841 |
| hgdp | rs7159841 |
| ensembl | rs7159841 |
| geneview | rs7159841 |
| scholar | rs7159841 |
| rs7159841 | |
| pharmgkb | rs7159841 |
| gwascentral | rs7159841 |
| openSNP | rs7159841 |
| 23andMe | rs7159841 |
| SNPshot | rs7159841 |
| SNPdbe | rs7159841 |
| MSV3d | rs7159841 |
| GWAS Ctlg | rs7159841 |
| GMAF | 0.2971 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 1.9999999999999999E-7 |
| Odds Ratio | NR NR |
[PMID 17903302] Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.
