rs1397048
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1397048(A;A) |
| Make rs1397048(A;G) |
| Make rs1397048(G;G) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 11 |
| Position | 56698623 |
| Gene | OR9G1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1397048 |
| dbSNP (classic) | rs1397048 |
| ClinGen | rs1397048 |
| ebi | rs1397048 |
| HLI | rs1397048 |
| Exac | rs1397048 |
| Gnomad | rs1397048 |
| Varsome | rs1397048 |
| LitVar | rs1397048 |
| Map | rs1397048 |
| PheGenI | rs1397048 |
| Biobank | rs1397048 |
| 1000 genomes | rs1397048 |
| hgdp | rs1397048 |
| ensembl | rs1397048 |
| geneview | rs1397048 |
| scholar | rs1397048 |
| rs1397048 | |
| pharmgkb | rs1397048 |
| gwascentral | rs1397048 |
| openSNP | rs1397048 |
| 23andMe | rs1397048 |
| SNPshot | rs1397048 |
| SNPdbe | rs1397048 |
| MSV3d | rs1397048 |
| GWAS Ctlg | rs1397048 |
| GMAF | 0.466 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | 7.0000000000000005E-8 |
| Odds Ratio | NR NR |
[PMID 20369022] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
