Variant: rs2505506 

    present in Gene: CSGALNACT2
    present in Chromosome: 10
    Position on Chromosome: 43150406
    Alleles of this Variant: C/G;T

rs2505506 in CSGALNACT2 gene and Hirschsprung Disease PMID 19196962 2009 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.