| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1811 | missense_variant | TBX20 | NM_001077653.2:c.526G>A | A | isolated CHD: ASD |
| S1812 | missense_variant | TBX20 | NM_001077653.2:c.526G>A | A | isolated CHD: ASD |
| S1813 | missense_variant | TBX20 | NM_001077653.2:c.526G>A | A | isolated CHD: ASD |