| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4908 | intron_variant | TBX20 | NC_000007.14:g.35236224C>G | C/C | isolated CHD: HLHS |
| S4909 | intron_variant | TBX20 | NC_000007.14:g.35236224C>G | C/G | isolated CHD: HLHS |
| S4910 | intron_variant | TBX20 | NC_000007.14:g.35236224C>G | G/G | isolated CHD: HLHS |
| S4911 | intron_variant | TBX20 | NC_000007.14:g.35236224C>G | C/G+G/G | isolated CHD: HLHS |
| S4912 | intron_variant | TBX20 | NC_000007.14:g.35236224C>G | C/G+C/C | isolated CHD: HLHS |
| S4913 | intron_variant | TBX20 | NC_000007.14:g.35236224C>G | C | isolated CHD: HLHS |