Variant: rs267607100 

    present in Gene: TAB2
    present in Chromosome: 6
    Position on Chromosome: 149378603
    Alleles of this Variant: C/A

rs267607100 in TAB2 gene and CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2 PMID 20493459 2010 Haploinsufficiency of TAB2 causes congenital heart defects in humans.