| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0652 | intron_variant | TFAP2B | NM_003221.4:c.539+62G>C | G/G | isolated CHD: PDA |
| S0653 | intron_variant | TFAP2B | NM_003221.4:c.539+62G>C | G/C | isolated CHD: PDA |
| S0654 | intron_variant | TFAP2B | NM_003221.4:c.539+62G>C | C/C | isolated CHD: PDA |