rs61748478(A;G)
From SNPedia
carrier of a Von Willebrand disease allele |
Is a | genotype |
of | rs61748478 |
Gene | VWF |
Chromosome | 12 |
Position | 6,044,349 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(A;G) | 3 | carrier of a Von Willebrand disease allele |
(G;G) | 4 | Von Willebrand disease, type 2N |
see discussion at rs61748478