| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0809 | missense_variant | ANK3 | NM_001149.3:c.2380G>T | T | isolated CHD: ASD |
| S0839 | missense_variant | ANK3 | NM_001149.3:c.2380G>T | T | isolated CHD: ASD |
| S0860 | missense_variant | ANK3 | NM_001149.3:c.2380G>T | T | isolated CHD: ASD |