rs216321
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common on affy axiom data |
| Make rs216321(C;T) |
| Make rs216321(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 6034818 |
| Gene | VWF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs216321 |
| dbSNP (classic) | rs216321 |
| ClinGen | rs216321 |
| ebi | rs216321 |
| HLI | rs216321 |
| Exac | rs216321 |
| Gnomad | rs216321 |
| Varsome | rs216321 |
| LitVar | rs216321 |
| Map | rs216321 |
| PheGenI | rs216321 |
| Biobank | rs216321 |
| 1000 genomes | rs216321 |
| hgdp | rs216321 |
| ensembl | rs216321 |
| geneview | rs216321 |
| scholar | rs216321 |
| rs216321 | |
| pharmgkb | rs216321 |
| gwascentral | rs216321 |
| openSNP | rs216321 |
| 23andMe | rs216321 |
| SNPshot | rs216321 |
| SNPdbe | rs216321 |
| MSV3d | rs216321 |
| GWAS Ctlg | rs216321 |
| GMAF | 0.1028 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18598365
] Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia.
[PMID 22568520] von Willebrand factor plasma levels, genetic variations and coronary heart disease in an older population.
[PMID 25779970] Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans
