| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0811 | missense_variant | ADGRB2 | NM_001294335.2:c.608G>T | T | isolated CHD: ASD |
| S0841 | missense_variant | ADGRB2 | NM_001294335.2:c.608G>T | T | isolated CHD: ASD |
| S0862 | missense_variant | ADGRB2 | NM_001294335.2:c.608G>T | T | isolated CHD: ASD |