| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3832 | missense_variant | NOS3 | NM_000603.5:c.894T>G | G/G | isolated CHD: VSD/ASD/TOF |
| S3833 | missense_variant | NOS3 | NM_000603.5:c.894T>G | T/G | isolated CHD: VSD/ASD/TOF |
| S3834 | missense_variant | NOS3 | NM_000603.5:c.894T>G | T/T | isolated CHD: VSD/ASD/TOF |
| S3835 | missense_variant | NOS3 | NM_000603.5:c.894T>G | T/G+T/T | isolated CHD: VSD/ASD/TOF |
| S3836 | missense_variant | NOS3 | NM_000603.5:c.894T>G | G | isolated CHD: VSD/ASD/TOF |
| S3837 | missense_variant | NOS3 | NM_000603.5:c.894T>G | T | isolated CHD: VSD/ASD/TOF |