rs7714670
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs7714670(C;C) |
| Make rs7714670(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 73776529 |
| Gene | ARHGEF28 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7714670 |
| dbSNP (classic) | rs7714670 |
| ClinGen | rs7714670 |
| ebi | rs7714670 |
| HLI | rs7714670 |
| Exac | rs7714670 |
| Gnomad | rs7714670 |
| Varsome | rs7714670 |
| LitVar | rs7714670 |
| Map | rs7714670 |
| PheGenI | rs7714670 |
| Biobank | rs7714670 |
| 1000 genomes | rs7714670 |
| hgdp | rs7714670 |
| ensembl | rs7714670 |
| geneview | rs7714670 |
| scholar | rs7714670 |
| rs7714670 | |
| pharmgkb | rs7714670 |
| gwascentral | rs7714670 |
| openSNP | rs7714670 |
| 23andMe | rs7714670 |
| SNPshot | rs7714670 |
| SNPdbe | rs7714670 |
| MSV3d | rs7714670 |
| GWAS Ctlg | rs7714670 |
| GMAF | 0.377 |
| 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 | A |
| P-val | 2E-9 |
| Odds Ratio | 1.52 [NR] |
| ClinVar | |
|---|---|
| Risk | rs7714670(C;C) |
| Alt | rs7714670(C;C) |
| Reference | Rs7714670(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | ARHGEF28 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000005.9:g.73072354T>C |
| CLNSRC | |
| CLNACC | RCV000243131.1, |
