| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0824 | missense_variant | FOCAD | NM_017794.4:c.5333C>T | T | isolated CHD: ASD |
| S0837 | missense_variant | FOCAD | NM_017794.4:c.5333C>T | T | isolated CHD: ASD |
| S0854 | missense_variant | FOCAD | NM_017794.4:c.5333C>T | T | isolated CHD: ASD |
| S0875 | missense_variant | FOCAD | NM_017794.4:c.5333C>T | T | isolated CHD: ASD |
| S0886 | missense_variant | FOCAD | NM_017794.4:c.5333C>T | T | isolated CHD: ASD |