| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1596 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | A/A | isolated CHD: ASD/VSD/TOF |
| S1597 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | G/A | isolated CHD: ASD/VSD/TOF |
| S1598 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | G/G | isolated CHD: ASD/VSD/TOF |