Variant: rs17189763 

    present in Gene: HCG21
    present in Chromosome: 6
    Position on Chromosome: 30955750
    Alleles of this Variant: C/T

rs17189763 in HCG21 gene and CONOTRUNCAL HEART MALFORMATIONS (disorder) PMID 28468790 2017 Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.