Variant: rs10950690 

    present in Gene: SNX13
    present in Chromosome: 7
    Position on Chromosome: 17941687
    Alleles of this Variant: C/A;G

rs10950690 in SNX13 gene and Fibrinogen assay PMID 28107422 2017 Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.