| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1635 | intron_variant | FMN1 | NC_000015.10:g.32800761G>A | A/A | isolated CHD: ASD |
| S1636 | intron_variant | FMN1 | NC_000015.10:g.32800761G>A | A/G | isolated CHD: ASD |
| S1637 | intron_variant | FMN1 | NC_000015.10:g.32800761G>A | G/G | isolated CHD: ASD |