| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4706 | missense_variant | GSTO1 | NM_004832.3:c.419C>A | C/C | NA: NA |
| S4707 | missense_variant | GSTO1 | NM_004832.3:c.419C>A | C/A | NA: NA |
| S4708 | missense_variant | GSTO1 | NM_004832.3:c.419C>A | A/A | NA: NA |
| S4709 | missense_variant | GSTO1 | NM_004832.3:c.419C>A | C/A+A/A | NA: NA |