rs216311
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs216311(A;G) |
| Make rs216311(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 6019277 |
| Gene | VWF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs216311 |
| dbSNP (classic) | rs216311 |
| ClinGen | rs216311 |
| ebi | rs216311 |
| HLI | rs216311 |
| Exac | rs216311 |
| Gnomad | rs216311 |
| Varsome | rs216311 |
| LitVar | rs216311 |
| Map | rs216311 |
| PheGenI | rs216311 |
| Biobank | rs216311 |
| 1000 genomes | rs216311 |
| hgdp | rs216311 |
| ensembl | rs216311 |
| geneview | rs216311 |
| scholar | rs216311 |
| rs216311 | |
| pharmgkb | rs216311 |
| gwascentral | rs216311 |
| openSNP | rs216311 |
| 23andMe | rs216311 |
| SNPshot | rs216311 |
| SNPdbe | rs216311 |
| MSV3d | rs216311 |
| GWAS Ctlg | rs216311 |
| GMAF | 0.27 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23114148] [A1381T and -1793G/C Polymorphisms of vWF Gene Impact the Plasma vWF Levels in Yugur, Tibetan and Han Nationalities of China]
[PMID 23358615] Changes of plasma vWF level in response to the improvement of air quality: an observation of 114 healthy young adults.
| ClinVar | |
|---|---|
| Risk | rs216311(G;G) |
| Alt | rs216311(G;G) |
| Reference | Rs216311(A;A) |
| 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.6128443T>C |
| CLNSRC | |
| CLNACC | RCV000251458.1, RCV000337059.1, |
