rs61748497(C;T)
From SNPedia
carrier of a Von Willebrand disease allele |
Is a | genotype |
of | rs61748497 |
Gene | VWF |
Chromosome | 12 |
Position | 6,025,624 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(C;C) | 4 | Von Willebrand disease, type 2N |
(C;T) | 3 | carrier of a Von Willebrand disease allele |
(T;T) | 0 | common in clinvar |
see discussion at rs61748497