| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1644 | intron_variant | FMN1 | NC_000015.10:g.32800761G>A | A/A | isolated CHD: ASD/VSD/TOF |
| S1645 | intron_variant | FMN1 | NC_000015.10:g.32800761G>A | A/G | isolated CHD: ASD/VSD/TOF |
| S1646 | intron_variant | FMN1 | NC_000015.10:g.32800761G>A | G/G | isolated CHD: ASD/VSD/TOF |