Variant: rs1057515420 

    present in Gene: EPHB4
    present in Chromosome: 7
    Position on Chromosome: 100819874
    Alleles of this Variant: G/A

rs1057515420 in EPHB4 gene and Tetralogy of Fallot PMID 27760138 2016 Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.

PMID 19597493 2009 De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.