Variant: rs671600 

    present in Gene: KIR2DS4;KIR2DS1;KIR2DL1;KIR3DL1
    present in Chromosome: 19
    Position on Chromosome: 54845969
    Alleles of this Variant: T/C

rs671600 in KIR2DS4;KIR2DS1;KIR2DL1;KIR3DL1 gene and Hirschsprung Disease PMID 19196962 2009 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.