Variant: rs16879552 

    present in Gene: NRG1
    present in Chromosome: 8
    Position on Chromosome: 32553698
    Alleles of this Variant: C/T

rs16879552 in NRG1 gene and Congenital Intestinal Aganglionosis PMID 19196962 2009 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.

rs16879552 in NRG1 gene and Hirschsprung Disease PMID 19196962 2009 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.