Variant: rs4366490 

    present in Gene: SLC22A10;SLC22A24
    present in Chromosome: 11
    Position on Chromosome: 63145382
    Alleles of this Variant: T/C

rs4366490 in SLC22A10;SLC22A24 gene and CONOTRUNCAL HEART MALFORMATIONS (disorder) PMID 24800985 2014 Genome-wide association study of maternal and inherited loci for conotruncal heart defects.

rs4366490 in SLC22A10;SLC22A24 gene and Conotruncal defect PMID 24800985 2014 Genome-wide association study of maternal and inherited loci for conotruncal heart defects.