| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3962 | missense_variant | MTHFR | NM_005957.5:c.1298A>C | A/A | non-isolated CHD: TS, VSD |
| S3963 | missense_variant | MTHFR | NM_005957.5:c.1298A>C | A/C | non-isolated CHD: TS, VSD |
| S3964 | missense_variant | MTHFR | NM_005957.5:c.1298A>C | C/C | non-isolated CHD: TS, VSD |
| S3965 | missense_variant | MTHFR | NM_005957.5:c.1298A>C | A | non-isolated CHD: TS, VSD |
| S3966 | missense_variant | MTHFR | NM_005957.5:c.1298A>C | C | non-isolated CHD: TS, VSD |