| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0822 | missense_variant | TBC1D9B | NM_015043.4:c.686C>G | G | isolated CHD: ASD |
| S0852 | missense_variant | TBC1D9B | NM_015043.4:c.686C>G | G | isolated CHD: ASD |
| S0873 | missense_variant | TBC1D9B | NM_015043.4:c.686C>G | G | isolated CHD: ASD |
| S0885 | missense_variant | TBC1D9B | NM_015043.4:c.686C>G | G | isolated CHD: ASD |
| S0898 | missense_variant | TBC1D9B | NM_015043.4:c.686C>G | G | isolated CHD: ASD |