rs1063857
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs1063857(C;C) |
| Make rs1063857(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 6044348 |
| Gene | VWF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1063857 |
| dbSNP (classic) | rs1063857 |
| ClinGen | rs1063857 |
| ebi | rs1063857 |
| HLI | rs1063857 |
| Exac | rs1063857 |
| Gnomad | rs1063857 |
| Varsome | rs1063857 |
| LitVar | rs1063857 |
| Map | rs1063857 |
| PheGenI | rs1063857 |
| Biobank | rs1063857 |
| 1000 genomes | rs1063857 |
| hgdp | rs1063857 |
| ensembl | rs1063857 |
| geneview | rs1063857 |
| scholar | rs1063857 |
| rs1063857 | |
| pharmgkb | rs1063857 |
| gwascentral | rs1063857 |
| openSNP | rs1063857 |
| 23andMe | rs1063857 |
| SNPshot | rs1063857 |
| SNPdbe | rs1063857 |
| MSV3d | rs1063857 |
| GWAS Ctlg | rs1063857 |
| GMAF | 0.3434 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20940418] Variation in the von Willebrand Factor gene is associated with VWF levels and with the risk of cardiovascular disease
| ClinVar | |
|---|---|
| Risk | rs1063857(C;C) |
| Alt | rs1063857(C;C) |
| Reference | Rs1063857(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | not specified von Willebrand disorder |
| Variation | info |
| Gene | VWF |
| CLNDBN | not specified von Willebrand disorder |
| Reversed | 1 |
| HGVS | NC_000012.11:g.6153514A>G |
| CLNSRC | |
| CLNACC | RCV000242370.1, RCV000365333.1, |
