| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1659 | missense_variant | PITX2 | NM_000325.6:c.272G>A | A | isolated CHD: VSD |
| S1660 | missense_variant | PITX2 | NM_000325.6:c.272G>A | A | isolated CHD: VSD |
| S1661 | missense_variant | PITX2 | NM_000325.6:c.272G>A | A | isolated CHD: VSD |