| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2573 | missense_variant | NFATC1 | NM_006162.5:c.2251T>G | T/T | isolated CHD/non-isolated CHD: NA |
| S2574 | missense_variant | NFATC1 | NM_006162.5:c.2251T>G | G/T | isolated CHD/non-isolated CHD: NA |
| S2575 | missense_variant | NFATC1 | NM_006162.5:c.2251T>G | G/G | isolated CHD/non-isolated CHD: NA |