| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1632 | intron_variant | GPC5 | NC_000013.11:g.92342256C>A | A/A | isolated CHD: ASD/VSD/TOF |
| S1633 | intron_variant | GPC5 | NC_000013.11:g.92342256C>A | A/C | isolated CHD: ASD/VSD/TOF |
| S1634 | intron_variant | GPC5 | NC_000013.11:g.92342256C>A | C/C | isolated CHD: ASD/VSD/TOF |