rs1757948
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1757948(G;G) |
| Make rs1757948(G;T) |
| Make rs1757948(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 78695764 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1757948 |
| dbSNP (classic) | rs1757948 |
| ClinGen | rs1757948 |
| ebi | rs1757948 |
| HLI | rs1757948 |
| Exac | rs1757948 |
| Gnomad | rs1757948 |
| Varsome | rs1757948 |
| LitVar | rs1757948 |
| Map | rs1757948 |
| PheGenI | rs1757948 |
| Biobank | rs1757948 |
| 1000 genomes | rs1757948 |
| hgdp | rs1757948 |
| ensembl | rs1757948 |
| geneview | rs1757948 |
| scholar | rs1757948 |
| rs1757948 | |
| pharmgkb | rs1757948 |
| gwascentral | rs1757948 |
| openSNP | rs1757948 |
| 23andMe | rs1757948 |
| SNPshot | rs1757948 |
| SNPdbe | rs1757948 |
| MSV3d | rs1757948 |
| GWAS Ctlg | rs1757948 |
| GMAF | 0.2902 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21810271 ]
|
| Trait | |
| Title | Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. |
| Risk Allele | G |
| P-val | 0.000007 |
| Odds Ratio | 0.1500 [0.09-0.21] IU/dL increase |
