| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1146 | intron_variant | GDF1 | NC_000019.10:g.18878511T>C | C/C | isolated CHD: ASD |
| S1147 | intron_variant | GDF1 | NC_000019.10:g.18878511T>C | T/C | isolated CHD: ASD |
| S1148 | intron_variant | GDF1 | NC_000019.10:g.18878511T>C | T/T | isolated CHD: ASD |