| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0813 | missense_variant | FARP2 | NM_001282983.2:c.1174G>A | A | isolated CHD: ASD |
| S0843 | missense_variant | FARP2 | NM_001282983.2:c.1174G>A | A | isolated CHD: ASD |
| S0864 | missense_variant | FARP2 | NM_001282983.2:c.1174G>A | A | isolated CHD: ASD |
| S0879 | missense_variant | FARP2 | NM_001282983.2:c.1174G>A | A | isolated CHD: ASD |