| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2479 | missense_variant | MTHFR | NM_005957.5:c.677T>C | C/C | isolated CHD: PFO |
| S2480 | missense_variant | MTHFR | NM_005957.5:c.677T>C | C/T | isolated CHD: PFO |
| S2481 | missense_variant | MTHFR | NM_005957.5:c.677T>C | T/T | isolated CHD: PFO |