Variant: rs62472985 

    present in Gene: LOC101927378
    present in Chromosome: 7
    Position on Chromosome: 84567995
    Alleles of this Variant: C/G

rs62472985 in LOC101927378 gene and Congenital Intestinal Aganglionosis PMID 29379196 2018 Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.

rs62472985 in LOC101927378 gene and Hirschsprung Disease PMID 29379196 2018 Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.