rs61754002(A;C)
From SNPedia
carrier of a Von Willebrand disease allele |
Is a | genotype |
of | rs61754002 |
Gene | VWF |
Chromosome | 12 |
Position | 6,072,369 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;A) | 4 | Von Willebrand disease, type 2N |
(A;C) | 3 | carrier of a Von Willebrand disease allele |
(C;C) | 0 | common in clinvar |
see discussion at rs61754002