| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0825 | missense_variant | JMJD1C | NM_001282948.1:c.3826A>G | G | isolated CHD: ASD |
| S0855 | missense_variant | JMJD1C | NM_001282948.1:c.3826A>G | G | isolated CHD: ASD |
| S0876 | missense_variant | JMJD1C | NM_001282948.1:c.3826A>G | G | isolated CHD: ASD |