| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2668 | missense_variant | CASZ1 | NM_017766.5:c.113T>C | C | isolated CHD: VSD |
| S2669 | missense_variant | CASZ1 | NM_017766.5:c.113T>C | C | isolated CHD: VSD |
| S2670 | missense_variant | CASZ1 | NM_017766.5:c.113T>C | C | isolated CHD: VSD |