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 |