Variant: rs1864400 

    present in Gene: RET
    present in Chromosome: 10
    Position on Chromosome: 43114918
    Alleles of this Variant: G/A;T

rs1864400 in RET gene and Congenital Intestinal Aganglionosis PMID 25310821 2014 A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease.

rs1864400 in RET gene and Hirschsprung Disease PMID 25310821 2014 A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease.