| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1155 | intron_variant | GDF1 | NC_000019.10:g.18878511T>C | C/C | isolated CHD: PDA |
| S1156 | intron_variant | GDF1 | NC_000019.10:g.18878511T>C | T/C | isolated CHD: PDA |
| S1157 | intron_variant | GDF1 | NC_000019.10:g.18878511T>C | T/T | isolated CHD: PDA |