| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0655 | intron_variant | TFAP2B | NM_003221.4:c.601+5G>A | A | isolated CHD: PDA |
| S0656 | intron_variant | TFAP2B | NM_003221.4:c.601+5G>A | A | isolated CHD: PDA |
| S0657 | intron_variant | TFAP2B | NM_003221.4:c.601+5G>A | A | isolated CHD: PDA |
| S0658 | intron_variant | TFAP2B | NM_003221.4:c.601+5G>A | A | isolated CHD: PDA |
| S0659 | intron_variant | TFAP2B | NM_003221.4:c.601+5G>A | A | isolated CHD: PDA |