rs6771316
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6771316(A;A) |
| Make rs6771316(A;G) |
| Make rs6771316(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 72091381 |
| Gene | LINC00877 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6771316 |
| dbSNP (classic) | rs6771316 |
| ClinGen | rs6771316 |
| ebi | rs6771316 |
| HLI | rs6771316 |
| Exac | rs6771316 |
| Gnomad | rs6771316 |
| Varsome | rs6771316 |
| LitVar | rs6771316 |
| Map | rs6771316 |
| PheGenI | rs6771316 |
| Biobank | rs6771316 |
| 1000 genomes | rs6771316 |
| hgdp | rs6771316 |
| ensembl | rs6771316 |
| geneview | rs6771316 |
| scholar | rs6771316 |
| rs6771316 | |
| pharmgkb | rs6771316 |
| gwascentral | rs6771316 |
| openSNP | rs6771316 |
| 23andMe | rs6771316 |
| SNPshot | rs6771316 |
| SNPdbe | rs6771316 |
| MSV3d | rs6771316 |
| GWAS Ctlg | rs6771316 |
| GMAF | 0.112 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 5E-9 |
| Odds Ratio | 2.13 [NR] |
