| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0583 | intron_variant | NFATC1 | NM_006162.5:c.1920+56_1920+99dup | S/S | isolated CHD: Pm VSD |
| S0584 | intron_variant | NFATC1 | NM_006162.5:c.1920+56_1920+99dup | S/L | isolated CHD: Pm VSD |
| S0585 | intron_variant | NFATC1 | NM_006162.5:c.1920+56_1920+99dup | L/L | isolated CHD: Pm VSD |
| S0586 | intron_variant | NFATC1 | NM_006162.5:c.1920+56_1920+99dup | S/S+S/L | isolated CHD: Pm VSD |