| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1599 | intron_variant | NRP1 | NC_000010.11:g.33195901G>A | A/A | isolated CHD: ASD |
| S1600 | intron_variant | NRP1 | NC_000010.11:g.33195901G>A | A/G | isolated CHD: ASD |
| S1601 | intron_variant | NRP1 | NC_000010.11:g.33195901G>A | G/G | isolated CHD: ASD |