| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0933 | intron_variant | PTPN11 | NC_000012.12::g.112468611A>G | G/G | isolated CHD: TOF |
| S0934 | intron_variant | PTPN11 | NC_000012.12::g.112468611A>G | A/G | isolated CHD: TOF |
| S0935 | intron_variant | PTPN11 | NC_000012.12::g.112468611A>G | A/A | isolated CHD: TOF |
| S0936 | intron_variant | PTPN11 | NC_000012.12::g.112468611A>G | G/G | isolated CHD: TOF |
| S0937 | intron_variant | PTPN11 | NC_000012.12::g.112468611A>G | A/G | isolated CHD: TOF |
| S0938 | intron_variant | PTPN11 | NC_000012.12::g.112468611A>G | A/A | isolated CHD: TOF |