| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0817 | missense_variant | EPPK1 | NM_031308.4:c.4626G>T | T | isolated CHD: ASD |
| S0847 | missense_variant | EPPK1 | NM_031308.4:c.4626G>T | T | isolated CHD: ASD |
| S0868 | missense_variant | EPPK1 | NM_031308.4:c.4626G>T | T | isolated CHD: ASD |
| S0881 | missense_variant | EPPK1 | NM_031308.4:c.4626G>T | T | isolated CHD: ASD |