| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2446 | missense_variant | HAND2 | NM_021973.3:c.194G>T | G/T | isolated CHD: VSD |
| S2447 | missense_variant | HAND2 | NM_021973.3:c.194G>T | G/T | isolated CHD: VSD |
| S2449 | missense_variant | HAND2 | NM_021973.3:c.194G>T | G/T | isolated CHD: VSD |