| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1587 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | A/A | isolated CHD: ASD |
| S1588 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | G/A | isolated CHD: ASD |
| S1589 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | G/G | isolated CHD: ASD |