| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2702 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | T/T | isolated CHD: PDA |
| S2703 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | T/C | isolated CHD: PDA |
| S2704 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | C/C | isolated CHD: PDA |
| S2705 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | CC+CT/TT | isolated CHD: PDA |
| S2706 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | CC/CT+TT | isolated CHD: PDA |