Gene List:
ACTC1, ACVR2B, BCOR, BMPR2, BRAF, CBL, CHD7, CITED2, CRELD1, DNAH11, ELN, FLNA, FOXH1, GATA4, GATA5, GATA6, GDF1, GJA1, GPC3, HAND1, HAND2, HRAS, JAG1, KMT2D, KRAS, LEFTY2, MED13L, MMP21, MYH6, NKX2-5, NKX2-6, NODAL, NOTCH1, NOTCH2, NR2F2, NRAS, NSD1, PITX2, PKD1L1, PTPN11, RAF1, RBM10, RIT1, SALL4, SHOC2, SMAD6, SOS1, TAB2, TBX1, TBX20, TBX5, TFAP2B, TLL1, ZEB2, ZFPM2, ZIC3

References:
Paige S, et al. Whole Exome Sequencing for Diagnosis of Congenital Heart Disease. Circulation: Genomic and Precision Medicine.2018 Mar 19;11:null.

Szot JO, et al. A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. Circ Genom Precis Med. 2018;11:e001978.

Zaidi S, et al. Genetics and Genomics of Congential Heart Disease. Circulation Research. 2017;120:923–940.