rs9392653
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9392653(C;C) |
| Make rs9392653(C;T) |
| Make rs9392653(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 5071258 |
| Gene | LYRM4, LYRM4-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9392653 |
| dbSNP (classic) | rs9392653 |
| ClinGen | rs9392653 |
| ebi | rs9392653 |
| HLI | rs9392653 |
| Exac | rs9392653 |
| Gnomad | rs9392653 |
| Varsome | rs9392653 |
| LitVar | rs9392653 |
| Map | rs9392653 |
| PheGenI | rs9392653 |
| Biobank | rs9392653 |
| 1000 genomes | rs9392653 |
| hgdp | rs9392653 |
| ensembl | rs9392653 |
| geneview | rs9392653 |
| scholar | rs9392653 |
| rs9392653 | |
| pharmgkb | rs9392653 |
| gwascentral | rs9392653 |
| openSNP | rs9392653 |
| 23andMe | rs9392653 |
| SNPshot | rs9392653 |
| SNPdbe | rs9392653 |
| MSV3d | rs9392653 |
| GWAS Ctlg | rs9392653 |
| GMAF | 0.2406 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23509962 ]
|
| Trait | Venous thromboembolism (gene x gene interaction) |
| Title | A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. |
| Risk Allele | C |
| P-val | 2E-9 |
| Odds Ratio | 1.74 [NR] |
