| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0649 | 5_prime_UTR_variant | TFAP2B | NM_003221.4:c.1-34G>A | G/G | isolated CHD: PDA |
| S0650 | 5_prime_UTR_variant | TFAP2B | NM_003221.4:c.1-34G>A | G/A | isolated CHD: PDA |
| S0651 | 5_prime_UTR_variant | TFAP2B | NM_003221.4:c.1-34G>A | A/A | isolated CHD: PDA |
| S0660 | 5_prime_UTR_variant | TFAP2B | NM_003221.4:c.1-34G>A | A | isolated CHD: PDA |
| S0661 | 5_prime_UTR_variant | TFAP2B | NM_003221.4:c.1-34G>A | A | isolated CHD: PDA |