| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4682 | missense_variant | MTHFR | NM_005957.5:c.665C>T | C/C | NA: NA |
| S4683 | missense_variant | MTHFR | NM_005957.5:c.665C>T | C/T | NA: NA |
| S4684 | missense_variant | MTHFR | NM_005957.5:c.665C>T | T/T | NA: NA |
| S4685 | missense_variant | MTHFR | NM_005957.5:c.665C>T | C/T+T/T | NA: NA |