| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0918 | intron_variant | TGFβ2 | NC_000001.11:g.218347653A>G | A/A | isolated CHD: PDA |
| S0919 | intron_variant | TGFβ2 | NC_000001.11:g.218347653A>G | A/G | isolated CHD: PDA |
| S0920 | intron_variant | TGFβ2 | NC_000001.11:g.218347653A>G | G/G | isolated CHD: PDA |