Variant: rs121964895 

    present in Gene: VWF
    present in Chromosome: 12
    Position on Chromosome: 6021960
    Alleles of this Variant: C/A;T

rs121964895 in VWF gene and von Willebrand Disease PMID 31064749 2019 Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.