rs121964895(A;A)
From SNPedia
| Von Willebrand disease, type 1 |
| Is a | genotype |
| of | rs121964895 |
| Gene | VWF |
| Chromosome | 12 |
| Position | 6,021,960 |
| Merged from | Rs28934879 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 3 | Von Willebrand disease, type 1 |
| (A;G) | 3.5 | von Willebrand disease |
| (G;G) | 0 | common in clinvar |
see discussion at rs121964895
