Variant: rs10498632 

    present in Gene: TC2N
    present in Chromosome: 14
    Position on Chromosome: 91824400
    Alleles of this Variant: A/G

rs10498632 in TC2N gene and Venous Thromboembolism PMID 31420334 2019 Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.

rs10498632 in TC2N gene and von Willebrand's factor (lab test) PMID 30586737 2019 Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.