rs61750595(C;C)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs61750595 |
| Gene | VWF |
| Chromosome | 12 |
| Position | 6,018,443 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 3 | likely miscall in Ancestry V2.0 datasets; otherwise, carrier of a Von Willebrand disease allele |
| (T;T) | 4 | likely miscall in Ancestry V2.0 datasets; otherwise, Von Willebrand disease, type 3 |
