| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3826 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | G/G | isolated CHD: VSD/ASD/TOF |
| S3827 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | G/A | isolated CHD: VSD/ASD/TOF |
| S3828 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | A/A | isolated CHD: VSD/ASD/TOF |
| S3829 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | G/A+A/A | isolated CHD: VSD/ASD/TOF |
| S3830 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | G | isolated CHD: VSD/ASD/TOF |
| S3831 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | A | isolated CHD: VSD/ASD/TOF |