| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0818 | missense_variant | GAS2L2 | NM_139285.4:c.863C>T | T | isolated CHD: ASD |
| S0848 | missense_variant | GAS2L2 | NM_139285.4:c.863C>T | T | isolated CHD: ASD |
| S0869 | missense_variant | GAS2L2 | NM_139285.4:c.863C>T | T | isolated CHD: ASD |
| S0882 | missense_variant | GAS2L2 | NM_139285.4:c.863C>T | T | isolated CHD: ASD |