| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0823 | missense_variant | UVRAG | NM_003369.4:c.1922C>T | T | isolated CHD: ASD |
| S0836 | missense_variant | UVRAG | NM_003369.4:c.1922C>T | T | isolated CHD: ASD |
| S0853 | missense_variant | UVRAG | NM_003369.4:c.1922C>T | T | isolated CHD: ASD |
| S0874 | missense_variant | UVRAG | NM_003369.4:c.1922C>T | T | isolated CHD: ASD |