| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0921 | intron_variant | TGFβ2 | NC_000001.11:g.218347653A>G | A/A | isolated CHD: VSD |
| S0922 | intron_variant | TGFβ2 | NC_000001.11:g.218347653A>G | A/G | isolated CHD: VSD |
| S0923 | intron_variant | TGFβ2 | NC_000001.11:g.218347653A>G | G/G | isolated CHD: VSD |