| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0595 | intron_variant | NFATC1 | NM_006162.5:c.1920+56_1920+99dup | S/S | isolated CHD: valvulo septal defects |
| S0596 | intron_variant | NFATC1 | NM_006162.5:c.1920+56_1920+99dup | S/L | isolated CHD: valvulo septal defects |
| S0597 | intron_variant | NFATC1 | NM_006162.5:c.1920+56_1920+99dup | L/L | isolated CHD: valvulo septal defects |
| S0598 | intron_variant | NFATC1 | NM_006162.5:c.1920+56_1920+99dup | S/S+S/L | isolated CHD: valvulo septal defects |