| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0816 | missense_variant | ECE1 | NM_001113347.2:c.1525A>T | T | isolated CHD: ASD |
| S0834 | missense_variant | ECE1 | NM_001113347.2:c.1525A>T | T | isolated CHD: ASD |
| S0846 | missense_variant | ECE1 | NM_001113347.2:c.1525A>T | T | isolated CHD: ASD |
| S0867 | missense_variant | ECE1 | NM_001113347.2:c.1525A>T | T | isolated CHD: ASD |
| S0880 | missense_variant | ECE1 | NM_001113347.2:c.1525A>T | T | isolated CHD: ASD |