| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3844 | missense_variant | ACE | NM_000789.4:c.2350G>A | A/A | isolated CHD: VSD/ASD/TOF |
| S3845 | missense_variant | ACE | NM_000789.4:c.2350G>A | G/A | isolated CHD: VSD/ASD/TOF |
| S3846 | missense_variant | ACE | NM_000789.4:c.2350G>A | G/G | isolated CHD: VSD/ASD/TOF |
| S3847 | missense_variant | ACE | NM_000789.4:c.2350G>A | G/A+G/G | isolated CHD: VSD/ASD/TOF |
| S3848 | missense_variant | ACE | NM_000789.4:c.2350G>A | A | isolated CHD: VSD/ASD/TOF |
| S3849 | missense_variant | ACE | NM_000789.4:c.2350G>A | G | isolated CHD: VSD/ASD/TOF |