rs7306642
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7306642(A;A) |
| Make rs7306642(A;C) |
| Make rs7306642(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 103745256 |
| Gene | STAB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7306642 |
| dbSNP (classic) | rs7306642 |
| ClinGen | rs7306642 |
| ebi | rs7306642 |
| HLI | rs7306642 |
| Exac | rs7306642 |
| Gnomad | rs7306642 |
| Varsome | rs7306642 |
| LitVar | rs7306642 |
| Map | rs7306642 |
| PheGenI | rs7306642 |
| Biobank | rs7306642 |
| 1000 genomes | rs7306642 |
| hgdp | rs7306642 |
| ensembl | rs7306642 |
| geneview | rs7306642 |
| scholar | rs7306642 |
| rs7306642 | |
| pharmgkb | rs7306642 |
| gwascentral | rs7306642 |
| openSNP | rs7306642 |
| 23andMe | rs7306642 |
| SNPshot | rs7306642 |
| SNPdbe | rs7306642 |
| MSV3d | rs7306642 |
| GWAS Ctlg | rs7306642 |
| GMAF | 0.0753 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21810271 ]
|
| Trait | |
| Title | Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. |
| Risk Allele | A |
| P-val | 0.000003 |
| Odds Ratio | 0.3000 [0.18-0.42] IU/dL increase |
