| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4260 | intron_variant | TBX1 | NM_005992.1:c.1010-5255G>C | C/C | isolated CHD: VSD/ASD/PDA |
| S4261 | intron_variant | TBX1 | NM_005992.1:c.1010-5255G>C | G/C | isolated CHD: VSD/ASD/PDA |
| S4262 | intron_variant | TBX1 | NM_005992.1:c.1010-5255G>C | G/G | isolated CHD: VSD/ASD/PDA |