| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3440 | missense_variant | MTHFR | NM_005957.5:c.677T>C | C | isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD |
| S3441 | missense_variant | MTHFR | NM_005957.5:c.677T>C | T | isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD |
| S3442 | missense_variant | MTHFR | NM_005957.5:c.677T>C | C | isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD |
| S3443 | missense_variant | MTHFR | NM_005957.5:c.677T>C | T | isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD |