| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0819 | missense_variant | MYH6 | NM_002471.3:c.688G>C | C | isolated CHD: ASD |
| S0849 | missense_variant | MYH6 | NM_002471.3:c.688G>C | C | isolated CHD: ASD |
| S0870 | missense_variant | MYH6 | NM_002471.3:c.688G>C | C | isolated CHD: ASD |
| S0883 | missense_variant | MYH6 | NM_002471.3:c.688G>C | C | isolated CHD: ASD |
| S0897 | missense_variant | MYH6 | NM_002471.3:c.688G>C | C | isolated CHD: ASD |