| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2672 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | T/T | isolated CHD: ASD |
| S2673 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | T/C | isolated CHD: ASD |
| S2674 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | C/C | isolated CHD: ASD |
| S2675 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | CC+CT/TT | isolated CHD: ASD |
| S2676 | intron_variant | MIR196A2 | NC_000012.12:g.53991815C>T | CC/CT+TT | isolated CHD: ASD |