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.