Condition: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2


rs1531070 in MAML3 gene and CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2 PMID 23708190 2013 A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.

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