| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2095 | intron_variant | VEGFA | NC_000006.12:g.43774790G>A | G/G | isolated CHD: TOF |
| S2096 | intron_variant | VEGFA | NC_000006.12:g.43774790G>A | G/A | isolated CHD: TOF |
| S2097 | intron_variant | VEGFA | NC_000006.12:g.43774790G>A | A/A | isolated CHD: TOF |
| S2098 | intron_variant | VEGFA | NC_000006.12:g.43774790G>A | G/A+A/A | isolated CHD: TOF |