Variant: rs4672229 

    present in Gene: VRK2;LOC107984043
    present in Chromosome: 2
    Position on Chromosome: 58049145
    Alleles of this Variant: C/A;T

rs4672229 in VRK2;LOC107984043 gene and Congenital Intestinal Aganglionosis PMID 27702942 2016 Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

rs4672229 in VRK2;LOC107984043 gene and Hirschsprung Disease PMID 27702942 2016 Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.