| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4718 | missense_variant | CN2 | NM_000355.4:c.776G>C | C/C | NA: NA |
| S4719 | missense_variant | CN2 | NM_000355.4:c.776G>C | C/G | NA: NA |
| S4720 | missense_variant | CN2 | NM_000355.4:c.776G>C | G/G | NA: NA |
| S4721 | missense_variant | CN2 | NM_000355.4:c.776G>C | C/G + G/G | NA: NA |