rs61751296(C;T)
From SNPedia
| carrier of a Von Willebrand disease allele |
| Is a | genotype |
| of | rs61751296 |
| Gene | VWF |
| Chromosome | 12 |
| Position | 5,969,337 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 3 | carrier of a Von Willebrand disease allele |
| (T;T) | 4 | Von Willebrand disease, type 3 |
reported to be associated with Type 3 Von Willebrand disease; see discussion at rs61751296
