| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2597 | missense_variant | KDR | NM_002253.3:c.889G>A | G/G | isolated CHD/non-isolated CHD: NA |
| S2598 | missense_variant | KDR | NM_002253.3:c.889G>A | G/A | isolated CHD/non-isolated CHD: NA |
| S2599 | missense_variant | KDR | NM_002253.3:c.889G>A | A/A | isolated CHD/non-isolated CHD: NA |